Therapeutic uses of selected pyrimidine compounds with anti-mer tyrosine kinase activity

ABSTRACT

Uses of pyrimidines with anti-Mer tyrosine kinase activity as anti-infective agents, immunostimulatory and immunomodulatory agents, anti-cancer agents (including against MerTK −/− tumors and ITD and TKD mutant forms of Acute Myeloid Leukemia (AML)), and as adjunctive agents in combination with chemotherapeutic, radiation or other standard of care for neoplasms.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/978,268 filed Apr. 11, 2014, U.S. Provisional Application No. 61/978,281 filed Apr. 11, 2014, U.S. Provisional Application No. 61/978,290 filed Apr. 11, 2014, U.S. Provisional Application No. 61/978,321 filed Apr. 11, 2014, U.S. Provisional Application No. 61/978,443 filed Apr. 11, 2014, U.S. Provisional Application No. 61/978,485 filed Apr. 11, 2014, U.S. Provisional Application No. 61/978,513 filed Apr. 11, 2014, U.S. Provisional Application No. 61/994,384 filed May 16, 2014, and U.S. Provisional Application No. 62/088,159 filed Dec. 5, 2014. The entirety of each of these applications is hereby incorporated by reference for all purposes.

GOVERNMENT INTEREST

The U.S. Government has rights in this invention by virtue of support under Contract No. HHSN261200800001E awarded by the National Cancer Institute, National Institute of Health.

FIELD OF THE INVENTION

The present invention is directed to the use of selected pyrimidine compounds having Mer tyrosine kinase (MerTK) inhibitory activity as anti-infective agents, immunostimulatory and immunomodulatory agents, anti-cancer agents (including against MerTK −/− tumors and ITD and TKD mutant forms of Acute Myeloid Leukemia (AML)), and as adjunctive agents in combination with chemotherapeutic, radiation or other standard of care for neoplasms.

BACKGROUND OF THE INVENTION

MerTK is a member of a receptor tyrosine kinase (RTK) family known as TAM, which also includes AXL and TYRO3. Each member of the TAM family contains an extracellular domain, a transmembrane domain and a conserved intracellular kinase domain. MerTK was first discovered in the laboratory of H. Shelton Earp at the University of North Carolina in 1994 (Graham et al., Cloning and mRNA expression analysis of a novel human protooncogene, c-mer. Cell Growth Differ 5, 647-657 (1994)). The TAM family members undergo ligand-induced homodimerization, followed by catalytic tyrosine kinase activation and intracellular signaling. Cross-phosphorylation has also been demonstrated within this RTK family, suggesting heterodimerization can occur also. These RTKs are widely expressed in many epithelial tissues and in cells of the immune, nervous, and reproductive systems. MerTK was given its name by the Earp laboratory because it was found to be expressed in monocytes and in tissues of epithelial and reproductive tissue.

As described in more detail below, ligand-bound MerTK can complex with phosphatidyl serine and it binds apoptotic cells which triggers ingestion and suppresses inflammatory cytokines. It is aberrantly expressed in certain cancers (for example, acute leukemia (ALL and AML) and some solid tumors (for example melanoma, breast cancer, colon cancer, non-small cell lung carcinoma, glioblastoma and others).

The MerTK ligands include growth arrest-specific 6 protein (GAS6; Chen, et al; Oncogene (1997) 14, 2033-2039), protein-S, tubby and tubbylike protein-1 (TULPI), and galectin-3. Several of these ligands are present in serum and expressed locally in a number of tissues. These ligands bind to the extracellular domain of MerTK, resulting in tyrosine kinase activation.

Since the discovery of MerTK in the Earp laboratory in 1994, there has been a growing body of literature and patents that suggest the possibility of MerTK as a druggable target for a number of indications.

TAM receptor tyrosine kinases have been investigated for their involvement in certain infectious diseases. Shimojima, et al., reported the involvement of members of the Tyro3 receptor tyrosine kinase family, Axl, Dkt and MerTK, in the cell entry of filoviruses Ebolavirus and Marburgvirus, and concluded that each Tyro3 family member is likely a cell entry factor in the infection (“Tyro3 Family-mediated Cell Entry of Ebola and Marburg Viruses” Journal of Virology, October 2006 p. 10109-10116).

U.S. Pat. No. 8,415,361 to Lemke, et al. (claiming priority to a Nov. 9, 2007 provisional application), assigned to The Salk Institute for Biological Studies, describes the use of TAM receptor inhibitors as antimicrobials. In particular, the '361 patent reports that inhibition of the TAM pathway in virally infected macrophages from TAM triple knock-out mice leads to reduced levels of infection with a variety of pseudotyped viruses with either filoviral, retroviral or rhabdoviral glycoproteins. Brindley, et al., reported that in a bioinformatics-based screen for cellular genes that enhance Zaire ebolavirus (ZEBOV) transduction, AXL mRNA expression strongly correlated with ZEBOV infection (“Tyrosine kinase receptor Axl enhances entry of Zaire ebolavirus without direct interactions with the viral glycoprotein” Virology, 415 (2011) 83-84).

Morizono, et al, published that Gas6 mediates binding of the virus to target cells by bridging virion envelope phosphatidyl serine to Axl on the target cells. Replication of vaccinia virus, which was previously reported to use apoptotic mimicry to enter cells, is enhanced by Gas6, and Morizono asserts that these results reveal an alternative molecular mechanism of viral entry that can broaden host range and enhance infectivity of enveloped viruses (“The Soluble Serum Protein Gas6 Bridges Virion Envelope Phosphatidylserine to the TAM Receptor Tyrosine Kinase Axl to mediate Viral Entry” Cell Host & Microbe 9, 286-298, 2011). In 2014, Morizono and Chen reported that virus binding by viral envelope phosphatidyl serine is a viral entry mechanism generalized to a number of families of viruses (Morizono and Chen, “Role of Phosphatidyl Receptors in Enveloped Virus Infection”, J. Virology Vol 88(8), 4275-4290 (Jan. 29, 2014)).

WO2013/124324 filed by Amara et al. (priority date Feb. 21, 2012), and assigned to Institut National De La Sante et De La Recherche Medicale, reports that Dengue virus is mediated by the interaction between phosphatidylserine at the surface of the Dengue viral envelope and TAM receptors present at the surface of the host cell, and that such interaction can be blocked, thereby inhibiting entry of Dengue into host cells. They also report that the interaction between phosphatidyl serine and TAM receptors is used by other flaviviruses such as Yellow Fever, West Nile and perhaps Chikungunya. Amara focuses on antisense, siRNA and antibody approaches.

Similarly, Bhattacharayya et al., reports that several human viruses, for example Ebola, Dengue, and HIV, externalize PtdSer on their capsid during budding and use phosphatidylserine to bind to and activate TAM RTKs in the presence of TAM ligands, allowing entry of the virus into cells and furthermore, activation of MerTK in macrophages in response to viral particles expressing PtdSer stimulates an anti-inflammatory cytokine profile as if apoptotic material was being ingested, thereby inhibiting the anti-viral immune response. Bhattacharayya et al observe that TAM receptors are engaged by viruses to attenuate type 1 interferon signaling (“Enveloped viruses disable innate immune responses in dendritic cells by direct activation of TAM receptors”, Cell Host & Microbe 14, 136,-147 (2013)). See also Meertens, L. et al. The TIM and TAM families of phosphatidylserine receptors mediate dengue virus entry. Cell Host Microbe 12, 544-557, doi:10.1016/j.chom.2012.08.009 (2012). Mercer, J. & Helenius, A. Vaccinia virus uses macropinocytosis and apoptotic mimicry to enter host cells. Science 320, 531-535, doi:10.1126/science.1155164 (2008).

MerTK is ectopically expressed or overexpressed in a number of hematologic and epithelial malignant cells. Expression of MerTK and GAS6 correlates with poor prognosis and/or chemoresistance in these tumor types. The mechanisms by which increased MerTK signaling in tumor cells contributes to tumor malignancy, however, remain unclear.

WO2013/177168 and WO2014/085225, both titled “Pyrimidine Compounds for the Treatment of Cancer” filed by Wang, et al., and assigned to the University of North Carolina describe pyrimidines with MerTK inhibitory activity for the treatment of tumors such as myeloid leukemia, lymphoblastic leukemia, melanoma, breast, lung, colon, liver, gastric, kidney, ovarian, uterine and brain cancer, wherein the pyrimidines have the general structures below, with R substituents as defined in the those applications:

An important observation was made in 2013 that MerTK −/− knock-out mice are less susceptible to tumor growth than normal mice. MerTK is normally expressed in myeloid lineage cells where it acts to suppress pro-inflammatory cytokines following ingestion of apoptotic material. It was found that MerTK −/− leukocytes exhibit lower tumor cell-induced expression of wound healing cytokines (IL-10 and GAS6) and enhanced expression of acute inflammatory cytokines (IL-12 and IL-6). Further, intratumoral CD8+ lymphocytes are increased. The loss of MerTK in the tumor microenvironment in Mer−/− mice slowed the establishment, growth, and metastasis of mammary tumors and melanomas in immune competent, syngeneic mice. Cook, R. S. et al., MerTK inhibition in tumor leukocytes decreases tumor growth and metastasis, J Clin Invest 123, 3231-3242 (2013).

Linger et al. have also presented data demonstrating increased MerTK expression in E2A-PBX11 and other cytogenetic subgroups of B-acute lymphoblastic leukemia (B-ALL), and that MerTK inhibition may attenuate prosurvival and proliferation signaling. Linger et al., Mer receptor tyrosine kinase is a therapeutic target in pre-B-cell acute lymphoblastic leukemia, Blood, vol. 122(9):1599-1609, 2013. Lee-Sherick, et al. (“Efficacy of a Mer and Flt3 tyrosine kinase small molecule inhibitor, UNC1666, in acute myeloid leukemia”, Oncotarget, Advance Publications 2015 Feb. 10, 2015) have reported that UNC 1666 (a pyrrolopyrimidine) decreases oncogenic signaling and myeloid survival in AML.

TAM (Tyro3-Axl-Mer) receptor tyrosine kinases have also been investigated for their involvement in platelet aggregation. In 2004, Chen et al, from the Johnson & Johnson Pharmaceutical Research and Development, published that MerTK, presumably through activation by its ligand Gas6, participates in the regulation of platelet function in vitro and platelet-dependent thrombosis in vivo. Chen, et al, “Mer Receptor tyrosine Kinase Signaling Participates in Platelet Function”, Arterioscler. Thromv Vasc. Biol. 1118-1123 June 2004. Chen reported that PtdSer on aggregating platelets activates MerTK, helping to stabilize clot formation. MerTK knockout mice have decreased platelet aggregation while maintaining normal bleeding times and coagulation parameters. Consequently, these mice appear to be protected from thrombosis without concomitant increased spontaneous bleeding (see also Angelillo-Scherrer A et al., Role of Gas6 receptors in platelet signaling during thrombus stabilization and implications for antithrombotic therapy. J. Clin. Invest. 2005, 115 (2), 237-246).

In 2007, Sather, et al., reported that membrane-bound MerTK is cleaved in the extracellular domain via a metalloproteinase to produce a soluble MerTK that decreased platelet aggregation in vitro and prevented fatal collagen/epinephrine-induced thromboembolism. “A soluble form of the Mer receptor tyrosine kinase inhibits macrophage clearance of apoptotic cells and platelet aggregation”, Blood, Vol 109(3): 1026-1033).

In December 2013, Zhang, W., et al., published a comparison of the activity of forty seven 5-amidopyrimidine based compounds for treatment of thrombosis (“Discovery of Mer specific tyrosine kinase inhibitors for the treatment and prevention of thrombosis”, J. Med Chem. vol. 56:9693-9700, 2013). MerTK, Axl and Tyro3 IC₅₀ data were presented for the selected 5-amidopyrimidines, and observations about activity based on substitutions at the 5-amide and the 2- and 4-amino groups were discussed. The publication reported that the compound illustrated below appeared to have a particularly good activity profile:

In December 2013, Zhang, W., et al., also published a comparison of the activity of forty six 5-arylpyrimidine based compounds for treatment of tumors “(Pseudo-cyclization through intramolecular hydrogen bond enables discovery of pyridine substituted pyrimidines as new Mer kinase inhibitors”, J. Med Chem., vol. 56:9683-9692, 2013). MerTK, Axl and Tyro3 IC₅₀ data were presented for the selected 5-arylpyrimidines, and observations about activity based on substitutions at the 5-aryl and the 2- and 4-amino groups were discussed. Zhang, et al. highlighted UNC2250 as a potential lead compound:

Paolino et al. have reported on the treatment of wild-type NK cells with a newly developed small molecule TAM kinase inhibitor, LDC1267, that conferred therapeutic potential and efficiently enhancing anti-metastatic NK cell activity in vivo. Oral or intraperitoneal administration using this TAM inhibitor markedly reduced murine mammary cancer and melanoma metastases dependent on NK cells. See, Paolino, M., et al., The E3 ligase Cbl-b and TAM receptors regulate cancer metastasis via natural killer cells, Nature, vol. 507:508-512, 2014. LDC1267 is a highly selective TAM kinase inhibitor with IC₅₀ of <5 nM, 8 nM, and 29 nM for MerTK, Tyro3, and Axl, respectively, and has the chemical structure:

Bernsmeier, et al., have noted that characteristics of decompensated cirrhosis and acute-on-chronic liver failure (ACLF) include susceptibility to infection, immune paresis and monocyte dysfunction. The authors found that the number of monocytes and macrophages that expressed MerTK was greatly increased in circulation, livers and lymph nodes of patients with ACLF. They found that addition of a substituted pyrazolopyrimidine UNC569 (see WO 2011/146313 filed by Wang, et al., and assigned to University of North Carolina at Chapel Hill, page 25) restored production of inflammatory cytokines. Bernsmeier, et al., “Patients with Acute-on-Chronic Liver Failure Have Increased Numbers of Regulatory Immune Cells Expressing the Receptor Tyrosine Kinase MERTK”, Gastroenterology 2015; 1-13.

It is an object of the invention to identify new methods and compositions for the treatment of infectious diseases.

It is another object of the invention to identify new methods and compositions for the treatment of thrombosis.

It is another object of the invention to identify new methods and compositions for the treatment of a tumor, cancer or other neoplasm.

It is yet another object of the invention to identify new methods and compositions for the treatment of disorders that can be treated with immunosuppression, or which would benefit from immunostimulatory therapy.

SUMMARY OF THE INVENTION

The present invention is directed to the use of selected pyrimidine compounds having Mer tyrosine kinase (MerTK) inhibitory activity as anti-infective agents, immunostimulatory agents, anti-cancer agents (including against MerTK −/− tumors and ITD and TKD mutant forms of Acute Myeloid Leukemia (AML)), and as adjunctive agents in combination with chemotherapeutic, radiation or other standard of care for neoplasms.

An effective amount of the pyrimidinyl compounds described in Formulas I, II, III and IV below or other active compounds as otherwise provided herein can be used to treat a host bearing any virus-related infection where the virus has a virion envelope phosphatidyl serine that complexes with MerTK to achieve viral entry or is otherwise facilitated by MerTK in the infectious process. Nonlimiting examples of such viruses include, but are not limited to, Flaviviridae viruses, including Flavivirus (such as Yellow Fever, West Nile and Dengue), Hepacivirus (Hepatitis C virus, “HCV”), Pegivirus and Pestivirus (Bovine viral diarrhea virus); Filoviridae viruses, including Ebola viruses; Togaviridae viruses, including Chikungunya virus; Coronaviruses, such as SARS (Severe acute respiratory syndrome) and MERS (Middle East respiratory syndrome); Orthomyxoviridae viruses, for example influenza; Paramyxoviridae viruses, for example Respiratory syncytial virus (RSV), measles and mumps; and Caliciviridae viruses, including Lagovirus, Vesivirus, and Sapovirus and Norovirus (Norwalk-like virus), and Lentiviruses, for example, HIV. In one embodiment, the virus is an enveloped virus. In another embodiment, the virus is a non-enveloped virus.

It has also been discovered that an effective amount of the pyrimidinyl compounds described in Formulas I, II, III and IV below can be used to treat a host bearing a bacterial infection. In one embodiment, the bacteria treated is, for example, a Gram-negative bacilli (GNB), especially Escherichia coli, Gram-positive cocci (GPC), Staphylococcus aureus, Enterococcus faecalis, or Streptococcus pneumoniae. In one embodiment, the bacterial infection is associated with liver failure. In one embodiment, an active compound disclosed herein is administered in combination with an antibiotic or another anti-bacterial agent.

It has also been discovered that the compounds described herein can be used as immunomodulatory agents that reverse the MerTK-induced suppression of pro-inflammatory cytokines such as wound healing cytokines (IL-10 and GAS6) and enhance the expression of acute inflammatory cytokines (IL-12 and IL-6). In this way, the pyrimidine compounds can “re-normalize” or “re-program” the host microenvironment in the diseased tissue area to attack the diseased cells.

Taking advantage of the immunostimulatory activity of the compounds described herein, or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof, may be used for the treatment of a MERTK-negative (−/−) tumor or cancer, for example MERTK-negative (−/−) breast cancer.

As part of the invention, one or more of the compounds disclosed herein can be used as adjunctive antineoplastic therapy for its immunostimulatory effect as a means to increase the efficacy of the antineoplastic standard of care therapies, such as chemotherapeutic compounds or radiation.

Some of these pyrimidine compounds have dual Mer/Flt-3 inhibitory activity, as discussed in more detail below, and thus are useful in the treatment of tumors mediated by FLT-3 or which exhibit drug resistance or ITD and TKD mutations, such as certain forms of Acute Myeloid Leukemia (AML))

A portion of the compounds described as useful in the present inventions were first described in WO 2013/177168 and WO 2014/085225, both of which are incorporated by reference for all purposes. The present invention describes for the first time that these compounds, and the additional compounds described herein that are not in WO 2013/177168 and WO 2014/085225, are useful for medical applications not described in or flowing from these earlier published applications. Specifically, MerTK inhibitors useful in treating a disorder described herein have the structure of Formula I, II, III, or IV:

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof, wherein the R groups in the formulas above are defined as follows:

wherein:

ring A is a 5- or 6-membered heteroaryl group (for example, pyridyl, pyrimidyl, thiazol, furanyl, pyridazinyl, pyrazinyl, imidazol, etc.). The dashed lines are optional double bonds. X is N or O. Y is a carbon atom or an S or N heteroatom in ring A in any suitable location.

R¹ is —R⁵R⁶, where R⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R⁶ is cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkylcycloalkyl, alkylheterocycloalkyl, alkylaryl, alkylheteroaryl or alkyl, and wherein R⁶ is optionally substituted one, two or three times with independently selected polar groups;

R² is —R⁷R⁸, where R⁷ is a covalent bond or C₁ to C₃ alkyl and R⁸ is cycloalkyl, heterocycloalkyl, aryl, heteroaryl or alkyl, and wherein R⁸ is optionally substituted one, two or three times with independently selected polar groups;

R³ is selected from the group consisting of H, alkyl, aryl, arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times with independently selected polar groups;

or R² and R³ together form a linking group;

R⁴ is H, loweralkyl, halo, or loweralkoxy;

R¹¹ is —R¹⁵R¹⁶, where R¹⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R¹⁶ is hydrogen, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocycloalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, heteroarylalkyl, hydroxyl, alkoxy, haloalkoxy, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, or acyloxy, and wherein R¹⁶ is optionally substituted one, two, three, four or five times;

-   -   m=0, 1, 2 or 3;

R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, alkoxyalkyl, hydroxyalkyl or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times;

R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocylic ring that can be optionally substituted;

R¹³ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times;

or R¹² and R¹³ together form a linking group;

R⁹ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times (typically R⁹ is H);

R¹¹ and R¹⁴ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted;

R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted;

R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl;

R¹⁴ is hydrogen, alkyl or alkylaryl;

R¹⁹ is —R²⁰R²¹, where R²⁰ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R²¹ is hydrogen, alkyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocyclolalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, alkylheteroaryl, halo, hydroxyl, alkoxy, haloalkoxy, mercapto, alkyl-S(O)_(m)—, haloalkyl-S(O)_(m)—, alkenyl-S(O)_(m)—, alkynyl-S(O)_(m)—, cycloalkyl-S(O)_(m)—, cycloalkylalkyl-S(O)_(m)—, aryl-S(O)_(m)—, arylalkyl-S(O)_(m)—, heterocyclo-S(O)_(m)—, heterocycloalkyl-S(O)_(m), amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstitutedamino, acylamino, acyloxy, ester, amide, COOH, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, and wherein R²¹ is optionally substituted one, two or three times; or

two adjacent R¹⁹ groups can form an aryl or heteroaryl ring with the carbons that they are bonded to and can be optionally substituted;

p=0, 1 or 2;

with the proviso for Formula III that:

wherein if R⁹ and R¹³ with the nitrogen to which they are bonded do not form a heterocyclic group then one of R⁹ or R¹³ is hydrogen; and

wherein if R¹⁶ and R¹² with the nitrogen to which they are bonded do not form a heterocyclic group then one of R¹⁰ or R¹² is hydrogen; and

wherein if R¹² and R¹³ together form a linking group, then both R⁹ and R¹⁰ are hydrogen.

In some embodiments, R⁵ is a covalent bond. In other embodiments, R⁵ is C₁ to C₃ alkylene such as —CH₂— or R⁵ is a linker group (for example, sulfonamide, amide, etc.)

In some embodiments, R⁷ is a covalent bond; in other embodiments, R⁷ is C₁ to C₃ alkylene such as —CH₂—.

In some embodiments, R⁶ is phenyl, piperidyl, or C₁-C₈ alkyl, or C₃ to C₈ cycloalkyl, which phenyl, pipyridyl, alkyl, or cycloalkylalkyl is unsubstituted or substituted from 1 to 3 times with sulfono, halo, amino, nitro, alkyl, alkoxyl, haloalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl.

In some embodiments, wherein R⁸ is C₁-C₈ alkyl or cyclohexyl, which alkyl or cyclohexyl is unsubstituted or substituted from 1 to 3 times with hydroxyl or amino.

In some embodiments, R³ is C₁-C₈ alkyl, C₃-C₈ cycloalkyl, C₄-C₁₂ cycloalkylalkyl, C₃-C₈ heterocycloalkyl, C₄-C₁₂ heterocycloalkylalkyl, C₄-C₁₂ arylalkyl, C₄-C₁₂ heteroarylalkyl, each of which is unsubstituted or substituted from one to three times with hydroxyl, halo, or alkoxy.

In some embodiments, R⁴ is H.

In another aspect, new pyrimidine compounds having the uses described herein have a structure selected from the compounds of Table 1 below, or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

In another embodiment, the active compounds are selected from Formulas IVe, IVf, IVg, and IVh:

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof, wherein the R groups in the formulas above are defined further below.

Particular examples of Formulas IVe, IVf, IVg, and IVh include, but are not limited to, the following:

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

The present invention thus provides at least the following:

-   -   (a) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for use as an anti-infective         agent.     -   (b) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for use as an anti-viral         agent.     -   (c) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for use as an anti-bacterial         agent.     -   (d) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for use as an anti-infective         agent, in combination with an additional anti-infective agent.     -   (e) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for use as an anti-viral         agent, in combination with an additional anti-viral agent.     -   (f) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for use as an anti-bacterial         agent, in combination with an additional anti-bacterial agent.     -   (g) Use of any of the active compounds described herein, or a         pharmaceutically acceptable composition, salt, isotopic analog,         or prodrug thereof, for the treatment or prevention of an         infection that gains entry into the cell via phosphatidyl serine         or another mechanism mediated by MerTK, or which infection is         otherwise mediated by MerTK, for example a viral or bacterial         infection, as further described herein.     -   (h) Use of any of the active compounds described herein, or a         pharmaceutically acceptable composition, salt, isotopic analog,         or prodrug thereof, to treat a host that has an immunosuppressed         microenvironment surrounding diseased tissue, by re-programming         the microenvironment to a pro-inflammatory environment. As one         example, the host is in need of treatment because it has tumor         associated macrophages that are protecting tumor cells.     -   (i) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for adjunctive antineoplastic         therapy as a means to increase the efficacy of the         antineoplastic standard of care therapies, such as         chemotherapeutic compounds or radiation.     -   (j) Use of one or more of the compounds disclosed herein in an         effective immunostimulatory dosage for adjunctive antineoplastic         therapy as a means to increase the efficacy of the         antineoplastic standard of care therapies, such as         chemotherapeutic compounds or radiation, in combination with an         additional chemotherapeutic agent.     -   (k) Use of one or more of the compounds as described herein in         an effective dosage to treat a host with a tumor, including         cancer.     -   (l) Use of one or more of the compounds as described herein in         an effective dosage to treat a host with a selected MerTK (+/+)         tumor, including cancer.     -   (m) Use of one or more of the compounds as described herein in         an effective dosage to treat a host with a selected MerTK (−/−)         tumor, including cancer.     -   (n) Use of one or more of the compounds disclosed herein to         treat a host with acute myeloid leukemia (including FLT3-ITD         AML, FLT3-TKD AML, or AML having both FLT3-ITD and FLT3-TKD         mutations).     -   (o) Use of one or more of the compounds disclosed herein in         combination with a second chemotherapeutic agent in a subject         undergoing a therapeutic regime to treat a tumor, including         cancer.     -   (p) Use of any of the active compounds described herein, to         treat a host with a thrombotic or clotting disorder.     -   (q) A compound selected from the structures of Table 1 below, or         a pharmaceutically acceptable composition, salt, isotopic         analog, or prodrug thereof.     -   (r) A compound as described herein, for use in the manufacture         of a medicament for use in treating an infectious disease,         including a viral disease or a bacterial disease.     -   (s) A compound as described herein, for use in the manufacture         of a medicament for treatment of a tumor, including cancer.     -   (t) A compound as described herein, for use in the manufacture         of a medicament for treatment of a MerTK +/+ tumor, including         cancer.     -   (u) A compound as described herein, for use in the manufacture         of a medicament for treatment of a MerTK −/− tumor, including         cancer.     -   (v) A compound as described herein, for use in the manufacture         of a medicament for acute myeloid leukemia (including FLT3-ITD         AML, FLT3-TKD AML, or AML having both FLT3-ITD and FLT3-TKD         mutations).     -   (w) A compound as described herein, for use in the manufacture         of a medicament for immunostimulatory therapy.     -   (x) A compound as described herein, for use in the manufacture         of a medicament for immunomodulatory therapy.     -   (y) A compound as described herein, for use in the manufacture         of a medicament for immunostimulatory therapy in combination         with chemotherapeutic or radiation standard of care.     -   (z) A compound as described herein, for use in the manufacture         of a medicament for immunomodulatory therapy in combination with         chemotherapeutic or radiation standard of care.     -   (aa) A compound as described herein, for use in the manufacture         of a medicament for the treatment of a thrombotic or clotting         disorder.     -   (bb) A process for manufacturing a medicament as described         in (r) through (aa).     -   (cc) A pharmaceutical formulation comprising an effective         host-treating amount of a compound selected from the structures         of Table 1 as described herein, and pharmaceutically acceptable         salts and prodrugs thereof, together with a pharmaceutically         acceptable carrier or diluent.     -   (dd) Processes for the manufacture of a compound selected from         the structures of Table 1, and salts, compositions, and dosage         forms thereof.     -   (ee) Processes for the preparation of therapeutic products that         contain an effective amount of a compound selected from the         structures of Table 1 as described herein.

DETAILED DESCRIPTION 1. Terminology

Compounds are described using standard nomenclature. Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in the art to which this invention belongs.

The compounds in any of the Formulas described herein include enantiomers, mixtures of enantiomers, diastereomers, tautomers, racemates and other isomers, such as rotamers, as if each is specifically described.

The terms “a” and “an” do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item. The term “or” means “and/or”. Recitation of ranges of values are merely intended to serve as a shorthand method of referring individually to each separate value falling within the range, unless otherwise indicated herein, and each separate value is incorporated into the specification as if it were individually recited herein. The endpoints of all ranges are included within the range and independently combinable. All methods described herein can be performed in a suitable order unless otherwise indicated herein or otherwise clearly contradicted by context. The use of examples, or exemplary language (e.g., “such as”), is intended merely to better illustrate the invention and does not pose a limitation on the scope of the invention unless otherwise claimed.

Isotopic Substitution

In one embodiment, the present invention includes compounds of Formula I, II, II, or IV and additional active compounds described herein, and the use of these compounds with at least one desired isotopic substitution of an atom, at an amount above the natural abundance of the isotope, i.e., enriched. Isotopes are atoms having the same atomic number but different mass numbers, i.e., the same number of protons but a different number of neutrons.

Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, and chlorine, such as ²H, ³H, ¹¹C, ¹³C, ¹⁴C, ¹⁵N, ¹⁸F ³¹P, ³²P, ³⁵S, ³⁶CI, ¹²⁵I respectively. The invention includes various isotopically labeled compounds as defined herein, for example those into which radioactive isotopes, such as ³H, ¹³C, and ¹⁴C, are present. Such isotopically labelled compounds are useful in metabolic studies (with ¹⁴C), reaction kinetic studies (with, for example ²H or ³H), detection or imaging techniques, such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT) including drug or substrate tissue distribution assays, or in radioactive treatment of patients. In particular, an ¹⁸F labeled compound may be particularly desirable for PET or SPECT studies. Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.

By way of general example and without limitation, isotopes of hydrogen, for example, deuterium (²H) and tritium (³H) may be used anywhere in described structures. Alternatively or in addition, isotopes of carbon, e.g., ¹³C and ¹⁴C, may be used. A typical isotopic substitution is deuterium for hydrogen at one or more locations on the molecule to improve the performance of the drug, for example, the pharmacodynamics, pharmacokinetics, biodistribution, half-life, stability, AUC, Tmax, Cmax, etc. For example, the deuterium can be bound to carbon in a location of bond breakage during metabolism (an a-deuterium kinetic isotope effect) or next to or near the site of bond breakage (a β-deuterium kinetic isotope effect).

Isotopic substitutions, for example deuterium substitutions, can be partial or complete. Partial deuterium substitution means that at least one hydrogen is substituted with deuterium. In certain embodiments, the isotope is 90, 95 or 99% or more enriched in an isotope at any location of interest. In one embodiments deuterium is 90, 95 or 99% enriched at a desired location. Unless otherwise stated, the enrichment at any point is above natural abundance and enough to alter a detectable property of the drug in a human.

In one embodiment, the substitution of a hydrogen atom for a deuterium atom occurs within an R group when at least one of the variables within the R group is hydrogen (e.g., ²H or D) or alkyl (e.g., CD₃). For example, when any of R groups are, or contain for example through substitution, methyl or ethyl, the alkyl residue is typically deuterated, e.g., CD₃, CH₂CD₃ or CD₂CD₃. In certain other embodiments, when any of the above mentioned R groups are hydrogen, the hydrogen may be isotopically enriched as deuterium (i.e., ²H).

A dash (“-”) that is not between two letters or symbols is used to indicate a point of attachment for a substituent. For example, —(C═O)NH₂ is attached through carbon of the keto (C═O) group.

“Alkyl” as used herein alone or as part of another group, refers to a straight or branched chain hydrocarbon containing from 1 to 10 carbon atoms. In one embodiment, the alkyl contains from 1 to about 10 carbon atoms, more generally from 1 to about 6 carbon atoms or from 1 to about 4 carbon atoms. In certain embodiments, the alkyl is C₁-C₃ or C₁-C₈. The specified ranges as used herein indicate an alkyl group having each member of the range described as an independent species. For example, the term C₁-C₃ alkyl as used herein indicates a straight or branched alkyl group having from 1, 2, or 3 carbon atoms and is intended to mean that each of these is described as an independent species. For example, the term C₁-C₃alkyl as used herein indicates a straight or branched alkyl group having from 1, 2, or 3 carbon atoms and is intended to mean that each of these is described as an independent species. Representative examples of alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, 3-methylhexyl, 2,2-dimethylpentyl, 2,3-dimethylpentyl, n-heptyl, n-octyl, n-nonyl, n-decyl, and the like. “Lower alkyl” as used herein, is a subset of alkyl, in some embodiments typically, and refers to a straight or branched chain hydrocarbon group containing from 1 to 4 carbon atoms. Representative examples of lower alkyl include, but are not limited to, methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, and the like. The term “alkyl” or “loweralkyl” is intended to include both substituted and unsubstituted alkyl or loweralkyl unless otherwise indicated and these groups may be substituted with groups selected from halo (e.g., haloalkyl), alkyl, haloalkyl, hydroxyalkyl, alkenyl, alkynyl, cycloalkyl (including spiroalkyl, e.g., —C(CH₂)₂₋₄ spiroalkyl), cycloalkylalkyl, aryl, arylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, alkylheteroaryl, hydroxyl, alkoxy (thereby creating a polyalkoxy such as polyethylene glycol), alkenyloxy, alkynyloxy, haloalkoxy, cycloalkoxy, cycloalkylalkyloxy, aryloxy, arylalkyloxy, heterocyclooxy, heterocyclolalkyloxy, mercapto, alkyl-S(O)_(m), haloalkyl-S(O)_(m), alkenyl-S(O)_(m), alkynyl-S(O)_(m), cycloalkyl-S(O)_(m), cycloalkylalkyl-S(O)_(m), aryl-S(O)_(m), arylalkyl-S(O)_(m), heterocyclo-S(O)_(m), heterocycloalkyl-S(O)_(m), amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstituted-amino, acylamino, acyloxy, ester, amide, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, nitro or cyano where m=0, 1, 2 or 3. In one embodiment, alkyl or loweralkyl can be substituted with groups selected from a polar group, —(CH₂)_(m)—N(R⁵⁰)₂, —(CH₂)_(m)—NH(CH₂)_(m)R⁵⁰, —(CH₂)_(m)NH(CH₂)₂₋₃N(R⁵⁰)₂, —S(O)₂OR⁵⁰, —CONHNHR⁵⁰, aminosulfonyl —C(CH₂)₂R⁵⁰ wherein each R⁵⁰ is independently selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, heteroaryl, or heteroarylalkyl.

“Alkenyl” as used herein alone or as part of another group, refers to a straight or branched chain hydrocarbon containing from 1 to 10 carbon atoms (or in loweralkenyl 1 to 4 carbon atoms) which include 1 to 4 double bonds in the normal chain. Representative examples of alkenyl include, but are not limited to, vinyl, 2-propenyl, 3-butenyl, 2-butenyl, 4-pentenyl, 3-pentenyl, 2-hexenyl, 3-hexenyl, 2,4-heptadiene, and the like. The term “alkenyl” or “loweralkenyl” is intended to include both substituted and unsubstituted alkenyl and loweralkenyl unless otherwise indicated and these groups may be substituted with groups as described in connection with alkyl and loweralkyl above.

“Alkynyl” as used herein alone or as part of another group, refers to a straight or branched chain hydrocarbon containing from 1 to 10 carbon atoms (or in loweralkynyl 1 to 4 carbon atoms) which include 1 triple bond in the normal chain. Representative examples of alkynyl include, but are not limited to, 2-propynyl, 3-butynyl, 2-butynyl, 4-pentynyl, 3-pentynyl, and the like. The term “alkynyl” or “loweralkynyl” is intended to include both substituted and unsubstituted alkynyl or loweralkynyl unless otherwise indicated and these groups may be substituted with the same groups as set forth in connection with alkyl and loweralkyl above.

“Cycloalkyl” as used herein alone or as part of another group, refers to a saturated or partially unsaturated cyclic hydrocarbon group containing from 3, 4 or 5 to 6, 7 or 8 carbons (which carbons may be replaced in a heterocyclic group as discussed below). Representative examples of cycloalkyl include, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl. These rings may be optionally substituted with additional substituents as described herein such as halo or loweralkyl. The term “cycloalkyl” is generic and intended to include heterocyclic groups as discussed below unless specified otherwise. In one embodiment, as used herein, the term “cycloalkyl” refers to a saturated or unsaturated hydrocarbon mono- or multi-ring, e.g., fused, bridged, or spiro rings system having 3 to 15 carbon atoms (e.g., C₃-C₁₀). Examples of cycloalkyl include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and adamantyl. In another embodiment, the term “cycloalkyl” refers to a saturated or partially unsaturated, monocyclic, fused bicyclic or bridged polycyclic ring assembly containing from 3 to 12 ring atoms, or the number of atoms indicated. Cycloalkyl can include any number of carbons, such as C₃₋₆, C₄₋₆, C₅₋₆, C₃₋₈, C₄₋₈, C₅₋₈, and C₆₋₈. Saturated monocyclic cycloalkyl rings include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cyclooctyl. Saturated bicyclic and polycyclic cycloalkyl rings include, for example, norbornane, [2.2.2]bicyclooctane, decahydronaphthalene and adamantane. Cycloalkyl groups can also be partially unsaturated, having one or more double bonds in the ring. Representative cycloalkyl groups that are partially unsaturated include, but are not limited to, cyclobutene, cyclopentene, cyclohexene, cyclohexadiene (1,3- and 1,4-isomers), cycloheptene, cycloheptadiene, cyclooctene, cyclooctadiene (1,3-, 1,4- and 1,5-isomers), norbornene, and norbornadiene. These groups may be substituted with groups as described in connection with alkyl and loweralkyl above.

“Heterocyclic group” or “heterocyclo” as used herein alone or as part of another group, refers to an aliphatic (e.g., fully or partially saturated heterocyclo) or aromatic (e.g., heteroaryl) monocyclic- or a bicyclic-ring system. In some embodiments, monocyclic ring systems are exemplified by any 7 membered ring containing 1, 2, 3, or 4 heteroatoms independently selected from oxygen, nitrogen and sulfur. Monocyclic ring systems are exemplified by any 5 or 6 membered ring containing 1, 2, 3, or 4 heteroatoms independently selected from oxygen, nitrogen and sulfur. The 5 membered ring has from 0-2 double bonds and the 6 membered ring has from 0-3 double bonds. Representative examples of monocyclic ring systems include, but are not limited to, azetidine, azepine, aziridine, diazepine, 1,3-dioxolane, dioxane, dithiane, furan, imidazole, imidazoline, imidazolidine, isothiazole, isothiazoline, isothiazolidine, isoxazole, isoxazoline, isoxazolidine, morpholine, oxadiazole, oxadiazoline, oxadiazolidine, oxazole, oxazoline, oxazolidine, piperazine, piperidine, pyran, pyrazine, pyrazole, pyrazoline, pyrazolidine, pyridine, pyrimidine, pyridazine, pyrrole, pyrroline, pyrrolidine, tetrahydrofuran, tetrahydrothiophene, tetrazine, tetrazole, thiadiazole, thiadiazoline, thiadiazolidine, thiazole, thiazoline, thiazolidine, thiophene, thiomorpholine, thiomorpholine sulfone, thiopyran, triazine, triazole, trithiane, and the like. Bicyclic ring systems are exemplified by any of the above monocyclic ring systems fused to an aryl group as defined herein, a cycloalkyl group as defined herein, or another monocyclic ring system as defined herein. Representative examples of bicyclic ring systems include but are not limited to, for example, benzimidazole, benzothiazole, benzothiadiazole, benzothiophene, benzoxadiazole, benzoxazole, benzofuran, benzopyran, benzothiopyran, benzodioxine, 1,3-benzodioxole, cinnoline, indazole, indole, indoline, indolizine, naphthyridine, isobenzofuran, isobenzothiophene, isoindole, isoindoline, isoquinoline, phthalazine, purine, pyranopyridine, quinoline, quinolizine, quinoxaline, quinazoline, tetrahydroisoquinoline, tetrahydroquinoline, thiopyranopyridine, and the like. These rings include quaternized derivatives thereof and may be optionally substituted with groups selected from halo, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heterocyclo, heterocycloalkyl, hydroxyl, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, cycloalkoxy, cycloalkylalkyloxy, aryloxy, arylalkyloxy, heterocyclooxy, heterocyclolalkyloxy, mercapto, alkyl-S(O)_(m), haloalkyl-S(O)_(m), alkenyl-S(O)_(m), alkynyl-S(O)_(m), cycloalkyl-S(O)_(m), cycloalkylalkyl-S(O)_(m), aryl-S(O)_(m), arylalkyl-S(O)_(m), heterocyclo-S(O)_(m), heterocycloalkyl-S(O)_(m), amino, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH alkenylamino, alkynylamino, halo alkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstituted-amino, acylamino, acyloxy, ester, amide, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, nitro or cyano where m=0, 1, 2 or 3. In some embodiments, the heterocyclo groups can be substituted with groups as described in connection with alkyl and loweralkyl above. In another embodiment, the term “heterocyclo” refers to a saturated or unsaturated nonaromatic 3-8 membered monocyclic, 7-12 membered bicyclic (fused, bridged, or spiro rings), or 11-14 membered tricyclic ring system (fused, bridged, or spiro rings) having one or more heteroatoms (such as O, N, or S), unless specified otherwise. Examples of heterocyclo groups include, but are not limited to, piperidinyl, piperazinyl, pyrrolidinyl, dioxanyl, tetrahydrofuranyl, isoindolinyl, indolinyl, pyrazolidinyl, oxazolidinyl, isoxazolidinyl, triazolidinyl, tetrahyrofuranyl, oxiranyl, azetidinyl, oxetanyl, thietanyl, 1,2,3,6-tetrahydropyridinyl, tetrahydropyranyl, dihydropyranyl, pyranyl, morpholinyl, 1,4-diazepanyl, 1,4-oxazepanyl, 2-oxa-5-azabicyclo[2.2.1]heptanyl, 2,5-diazabicyclo[2.2.1]heptanyl, 2-oxa-6-azaspiro[3.3]heptanyl, 2,6-diazaspiro[3.3]heptanyl, 1,4-dioxa-8-azaspiro[4.5]decanyl and the like. These groups may be substituted with groups as described in connection with alkyl and loweralkyl above.

“Aryl” as used herein alone or as part of another group, refers to a monocyclic carbocyclic ring system or a bicyclic carbocyclic fused ring system having one or more aromatic rings. Representative examples of aryl include, azulenyl, indanyl, indenyl, naphthyl, phenyl, tetrahydronaphthyl, and the like. The term “aryl” is intended to include both substituted and unsubstituted aryl unless otherwise indicated and these groups may be substituted with the same groups as set forth in connection with alkyl and loweralkyl above.

“Arylalkyl” as used herein alone or as part of another group, refers to an aryl group, as defined herein, appended to the parent molecular moiety through an alkyl group, as defined herein. Representative examples of arylalkyl include, but are not limited to, benzyl, 2-phenylethyl, 3-phenylpropyl, 2-naphth-2-ylethyl, and the like.

“Heteroaryl” as used herein is as described in connection with heterocyclo above.

“Alkoxy” as used herein alone or as part of another group, refers to an alkyl or loweralkyl group, as defined herein (and thus including substituted versions such as polyalkoxy), appended to the parent molecular moiety through an oxy group, —O—. Representative examples of alkoxy include, but are not limited to, methoxy, ethoxy, propoxy, 2-propoxy, butoxy, tert-butoxy, pentyloxy, hexyloxy and the like.

“Halo” as used herein refers to any suitable halogen, including —F, —Cl, —Br, and —I.

“Mercapto” as used herein refers to an —SH group.

“Azido” as used herein refers to an —N₃ group.

“Cyano” as used herein refers to a —CN group.

“Formyl” as used herein refers to a —C(O)H group.

“Carboxylic acid” as used herein refers to a —C(O)OH group.

“Hydroxyl” as used herein refers to an —OH group.

“Nitro” as used herein refers to an —NO₂ group.

“Acyl” as used herein alone or as part of another group refers to a —C(O)R radical, where R is any suitable substituent such as aryl, alkyl, alkenyl, alkynyl, cycloalkyl or other suitable substituent as described herein.

“Alkylthio” as used herein alone or as part of another group, refers to an alkyl group, as defined herein, appended to the parent molecular moiety through a thio moiety, as defined herein. Representative examples of alkylthio include, but are not limited, methylthio, ethylthio, tert-butylthio, hexylthio, and the like.

“Amino” as used herein means the radical —NH₂.

“Alkylamino” as used herein alone or as part of another group means the radical —NHR, where R is an alkyl group.

“Arylalkylamino” as used herein alone or as part of another group means the radical —NHR, where R is an arylalkyl group.

“Disubstituted-amino” as used herein alone or as part of another group means the radical —NR_(a)R_(b), where R_(a) and R_(b) are independently selected from the groups hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heterocyclo, heterocycloalkyl.

“Acylamino” as used herein alone or as part of another group means the radical —NR_(a)R_(b), where R_(a) is an acyl group as defined herein and R_(b) is selected from the groups hydrogen, alkyl, haloalkyl, alkenyl, alkynyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl, heterocyclo, heterocycloalkyl.

“Acyloxy” as used herein alone or as part of another group means the radical —OR, where R is an acyl group as defined herein.

“Ester” as used herein alone or as part of another group refers to a —C(O)OR radical, where R is any suitable substituent such as alkyl, cycloalkyl, alkenyl, alkynyl or aryl.

“Amide” as used herein alone or as part of another group refers to a —C(O)NR_(a)R_(b) radical, where R_(a) and R_(b) are any suitable substituent such as alkyl, cycloalkyl, alkenyl, alkynyl or aryl. In some embodiments, R_(a) and R_(b) together with the nitrogen to which they are bonded form a heterocyclic ring.

“Sulfoxyl” as used herein refers to a compound of the formula —S(O)R, where R is any suitable substituent such as alkyl, cycloalkyl, alkenyl, alkynyl or aryl.

“Sulfonyl” as used herein refers to a compound of the formula —S(O)(O)R, where R is any suitable substituent such as amino, alkyl, cycloalkyl, alkenyl, alkynyl or aryl.

“Sulfonate” as used herein refers to a compound of the formula —S(O)(O)OR, where R is any suitable substituent such as alkyl, cycloalkyl, alkenyl, alkynyl or aryl.

“Sulfonic acid” as used herein refers to a compound of the formula —S(O)(O)OH.

“Sulfonamide” as used herein alone or as part of another group refers to a —S(O)₂NR_(a)R_(b) radical, where R_(a) and R_(b) are any suitable substituent such as H, alkyl, cycloalkyl, alkenyl, alkynyl or aryl. In some embodiments, R_(a) and R_(b) are any suitable substituent such as hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, heteroaryl, or heteroarylalkyl and each R_(a) and R_(b) can be optionally substituted one, two or three times. In some embodiments, R_(a) and R_(b) together with the nitrogen to which they are bonded form a heterocyclic ring that can be optionally substituted one, two or three times.

“Urea” as used herein alone or as part of another group refers to an N(R_(c))C(O)NR_(a)R_(b) radical, where R_(a), R_(b) and R_(c) are any suitable substituent such as H, alkyl, cycloalkyl, alkenyl, alkynyl or aryl. In some embodiments, R_(a) and R_(b) together with the nitrogen to which they are bonded form a heterocyclic ring.

“Alkoxyacylamino” as used herein alone or as part of another group refers to an —N(R_(a))C(O)OR_(b) radical, where R_(a), R_(b) are any suitable substituent such as H, alkyl, cycloalkyl, alkenyl, alkynyl or aryl.

“Aminoacyloxy” as used herein alone or as part of another group refers to an —OC(O)NR_(a)R_(b) radical, where R_(a) and R_(b) are any suitable substituent such as H, alkyl, cycloalkyl, alkenyl, alkynyl or aryl. In some embodiments, R_(a) and R_(b) together with the nitrogen to which they are bonded form a heterocyclic ring.

“Optionally substituted” as used herein refers to the optionally substitution of a chemical moiety. These moieties can be substituted with groups selected from, but not limited to, halo (e.g., haloalkyl), alkyl, haloalkyl, hydroxyalkyl, alkenyl, alkynyl, cycloalkyl (including spiroalkyl, e.g., —C(CH₂)₂₄ spiroalkyl), cycloalkylalkyl, aryl, arylalkyl, aryl substituted heteroaryl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, hydroxyl, alkoxy (thereby creating a polyalkoxy such as polyethylene glycol), alkenyloxy, alkynyloxy, haloalkoxy, cycloalkoxy, cycloalkylalkyloxy, aryloxy, arylalkyloxy, heterocyclooxy, heterocyclolalkyloxy, mercapto, alkyl-S(O)_(m), haloalkyl-S(O)_(m), alkenyl-S(O)_(m), alkynyl-S(O)_(m), cycloalkyl-S(O)_(m), cycloalkylalkyl-S(O)_(m), aryl-S(O)_(m), arylalkyl-S(O)_(m), heterocyclo-S(O)_(m), heterocycloalkyl-S(O)_(m), amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocyclo amino, heterocycloalkylamino, disubstituted-amino, acylamino, acyloxy, ester, amide, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, nitro, polar group or cyano where m=0, 1, 2 or 3. In one embodiment, alkyl or loweralkyl can be substituted with groups selected from a polar group, —(CH₂)_(m)—N(R⁵⁰)₂, —(CH₂)_(m)—NH(CH₂)_(m)R⁵⁰, —(CH₂)_(m)NH(CH₂)₂₋₃N(R⁵⁰)₂, —S(O)₂OR⁵⁰, —CONHNHR⁵⁰, aminosulfonyl —C(CH₂)₂R⁵⁰ wherein each R⁵⁰ is independently selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, heteroaryl, or heteroarylalkyl.

“Polar group” as used herein refers to a group wherein the nuclei of the atoms covalently bound to each other to form the group do not share the electrons of the covalent bond(s) joining them equally; that is the electron cloud is denser about one atom than another. This results in one end of the covalent bond(s) being relatively negative and the other end relatively positive; i.e., there is a negative pole and a positive pole. Examples of polar groups include, without limitations, halo, hydroxy, alkoxy, carboxy, nitro, cyano, amino (primary, secondary and tertiary), amido, ureido, sulfonamido, sulfinyl, sulfhydryl, silyl, S-sulfonamido, N-sulfonamido, C-carboxy, O-carboxy, C-amido, N-amido, sulfonyl, N-tert-butoxycarbonyl (or “t-BOC”) groups, phosphono, morpholino, piperazinyl, tetrazolo, and the like. See, e.g., U.S. Pat. No. 6,878,733, as well as alcohol, thiol, polyethylene glycol, polyol (including sugar, aminosugar, uronic acid), sulfonamide, carboxamide, hydrazide, N-hydroxycarboxamide, urea, metal chelates (including macrocyclic ligand or crown ether metal chelates). The polar group can be an ionic group.

“Ionic group” as used herein includes anionic and cationic groups, and includes groups (sometimes referred to as “ionogenic” groups) that are uncharged in one form but can be easily converted to ionic groups (for example, by protonation or deprotonation in aqueous solution). Examples include but are not limited to carboxylate, sulfonate, phosphate, amine, N-oxide, and ammonium (including quaternized heterocyclic amines such as imidazolium and pyridinium) groups. See, e.g., U.S. Pat. Nos. 6,478,863; 6,800,276; and 6,896,246. Additional examples include uronic acids, carboxylic acid, sulfonic acid, amine, and moieties such as guanidinium, phosphoric acid, phosphonic acid, phosphatidyl choline, phosphonium, borate, sulfate, etc.

“Deuterium” as used herein alone or as part of another group, refers to ²H, which has one proton and one neutron in the nucleus. It is a safe, non-radioactive isotope of hydrogen. Any hydrogen in a group or substituent described above may be replaced with deuterium to provide a “deuterated” compound, in some embodiments to modify and/or improve metabolic stability, resulting in better safety, tolerability and/or efficacy.

“Linking group” as used herein are generally bivalent aromatic, aliphatic, or mixed aromatic and aliphatic groups. Thus linking groups include linear or branched, substituted or unsubstituted aryl, alkyl, alkylaryl, or alkylarylalkyl linking groups, where the alkyl groups are saturated or unsaturated, and where the alkyl and aryl groups optionally containing independently selected heteroatoms such as 1, 2, 3 or 4 heteroatoms selected from the group consisting of N, O, and S. In some embodiments, linking groups containing from 2 to 20 carbon atoms are preferred. Numerous examples of suitable linking groups are known, including but not limited to those described in, U.S. Pat. Nos. 8,247,572; 8,097,609; 6,624,317; 6,613,345; 6,596,935; and 6,420,377, the disclosures of which are incorporated by reference herein in their entirety.

“Treat” as used herein refers to any type of treatment that imparts a benefit to a patient afflicted with a disease, including improvement in the condition of the patient (e.g., in one or more symptoms), delay in the progression of the disease, delay in onset of the disease, etc.

“Pharmaceutically acceptable” as used herein means that the compound or composition is suitable for administration to a subject to achieve the treatments described herein, without unduly deleterious side effects in light of the severity of the disease and necessity of the treatment.

A “dosage form” means a unit of administration of an active agent. Examples of dosage forms include tablets, capsules, injections, suspensions, liquids, emulsions, implants, particles, spheres, creams, ointments, suppositories, inhalable forms, transdermal forms, buccal, sublingual, topical, gel, mucosal, and the like.

“Pharmaceutical compositions” are compositions comprising at least one active agent, such as a compound or salt of Formula I, II, III, or IV, and at least one other substance, such as a carrier. “Pharmaceutical combinations” are combinations of at least two active agents which may be combined in a single dosage form or provided together in separate dosage forms with instructions that the active agents are to be used together to treat any disorder described herein.

“Pharmaceutically acceptable salts” includes derivatives of the disclosed compounds in which the parent compound is modified by making inorganic and organic, non-toxic, acid or base addition salts thereof. The salts of the present compounds can be synthesized from a parent compound that contains a basic or acidic moiety by conventional chemical methods. Generally, such salts can be prepared by reacting free acid forms of these compounds with a stoichiometric amount of the appropriate base (such as Na, Ca, Mg, or K hydroxide, carbonate, bicarbonate, or the like), or by reacting free base forms of these compounds with a stoichiometric amount of the appropriate acid. Such reactions are typically carried out in water or in an organic solvent, or in a mixture of the two. Generally, non-aqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are typical, where practicable. Salts of the present compounds further include solvates of the compounds and of the compound salts.

Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like. The pharmaceutically acceptable salts include the conventional non-toxic salts and the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids. For example, conventional non-toxic acid salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, mesylic, esylic, besylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, HOOC—(CH₂)_(n)—COOH where n is 0-4, and the like. Lists of additional suitable salts may be found, e.g., in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, Pa., p. 1418 (1985).

The term “carrier” applied to pharmaceutical compositions/combinations of the invention refers to a diluent, excipient, or vehicle with which an active compound is provided.

A “pharmaceutically acceptable excipient” means an excipient that is useful in preparing a pharmaceutical composition/combination that is generally safe, non-toxic and neither biologically nor otherwise inappropriate for administration to a host, and includes, in one embodiment, an excipient that is acceptable for veterinary use as well as human pharmaceutical use. A “pharmaceutically acceptable excipient” as used in the present application includes both one and more than one such excipient.

Compounds of the present invention may optionally be administered in conjunction with other compounds. The other compounds may optionally be administered concurrently. As used herein, the word “concurrently” means sufficiently close in time to produce a combined effect (that is, concurrently may be simultaneously, or it may be two or more events occurring within a short time period before or after each other).

The present invention is primarily focused on the treatment of a human subject or host, but the invention may be used to treat animals, such as mammalian subjects such as mice, rats, dogs, cats, livestock and horses for veterinary purposes, and for drug screening and drug development purposes. Subjects may be of any age, including infant, juvenile, adolescent, adult, and geriatric subjects.

2. Detailed Description of Compounds of Formula I, II, III, and IV

The present invention is directed to the use of selected pyrimidine compounds having Mer tyrosine kinase (MerTK) inhibitory activity as antinfective agents, immunostimulatory agents, anti-cancer agents (including against MerTK −/− tumors and ITD and TKD mutant forms of Acute Myeloid Leukemia (AML)), and as adjunctive agents in combination with chemotherapeutic, radiation or other standard of care for neoplasms, or as anti-thrombotic agents.

The majority of the compounds described as useful in the present invention were first described in WO 2013/177168 and WO 2014/085225, both of which are incorporated by reference for all purposes. The present invention describes for the first time that these compounds, and the additional compounds described herein that are not in WO 2013/177168 and WO 2014/085225, are useful for medical applications not described in these earlier published applications.

In one embodiment, the MerTK inhibitors useful in treating a disorder described herein have the structure of Formula I or II:

wherein:

ring A is a 5- or 6-membered heteroaryl group (for example, pyridyl, pyrimidyl, thiazol, furanyl, pyridazinyl, pyrazinyl, imidazol, etc.). The dashed lines are optional double bonds. X is N or O. Y is a carbon atom or an S or N heteroatom in ring A in any suitable location.

R¹ is —R⁵R⁶, where R⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R⁶ is cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkylcycloalkyl, alkylheterocycloalkyl, alkylaryl, alkylheteroaryl or alkyl, and wherein R⁶ is optionally substituted one, two or three times with independently selected polar groups;

R² is —R⁷R⁸, where R⁷ is a covalent bond or C₁ to C₃ alkyl and R⁸ is cycloalkyl, heterocycloalkyl, aryl, heteroaryl or alkyl, and wherein R⁸ is optionally substituted one, two or three times with independently selected polar groups;

R³ is selected from the group consisting of H, alkyl, aryl, arylalkyl, cycloalkylalkyl, heterocycloalkylalkyl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times with independently selected polar groups;

or R² and R³ together form a linking group;

R⁴ is H, loweralkyl, halo, or loweralkoxy;

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

In some embodiments, R⁵ is a covalent bond. In other embodiments, R⁵ is C₁ to C₃ alkylene such as —CH₂— or R⁵ is a linker group (for example, sulfonamide, amide, etc.).

In some embodiments, R⁷ is a covalent bond; in other embodiments, R⁷ is C₁ to C₃ alkylene such as —CH₂—.

In some embodiments, R⁶ is phenyl, piperidyl, or C₁-C₈ alkyl, or C₃ to C₈ cycloalkyl, which phenyl, pipyridyl, alkyl, or cycloalkylalkyl is unsubstituted or substituted from 1 to 3 times with sulfono, halo, amino, nitro, alkyl, alkoxyl, haloalkyl, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl.

In some embodiments, wherein R⁸ is C₁-C₈ alkyl or cyclohexyl, which alkyl or cyclohexyl is unsubstituted or substituted from 1 to 3 times with hydroxyl or amino.

In some embodiments, R³ is C₁-C₈ alkyl, C₃-C₈ cycloalkyl, C₄-C₁₂ cycloalkylalkyl, C₃-C₈ heterocycloalkyl, C₄-C₁₂ heterocycloalkylalkyl, C₄-C₁₂ arylalkyl, C₄-C₁₂ heteroarylalkyl, each of which is unsubstituted or substituted from one to three times with hydroxyl, halo, or alkoxy.

In some embodiments, R⁴ is H.

Particular examples of the foregoing include, but are not limited to:

including or pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cycloalkyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cyclohexyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is para-hydroxy cyclohexyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cycloalkyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cyclohexyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is para-hydroxy cyclohexyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cycloalkyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cyclohexyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is para-hydroxy cyclohexyl, and R³ is loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cycloalkyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cyclohexyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is para-hydroxy cyclohexyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cycloalkyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cyclohexyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is para-hydroxy cyclohexyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cycloalkyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cyclohexyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is para-hydroxy cyclohexyl, and R³ is butyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cycloalkyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cyclohexyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is para-hydroxy cyclohexyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cycloalkyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cyclohexyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is para-hydroxy cyclohexyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cycloalkyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cyclohexyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is para-hydroxy cyclohexyl, and R³ is cycloalkylalkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cycloalkyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cyclohexyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is para-hydroxy cyclohexyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cycloalkyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cyclohexyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is para-hydroxy cyclohexyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cycloalkyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is cyclohexyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heterocycloalkyl, R² is para-hydroxy cyclohexyl, and R³ is aryl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cycloalkyl, and R³ is phenyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is cyclohexyl, and R³ is phenyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is aryl, R² is para-hydroxy cyclohexyl, and R³ is phenyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cycloalkyl, and R³ is phenyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is cyclohexyl, and R³ is phenyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas Ia, IIa, IIb, and IIc, wherein R¹ is heteroaryl, R² is para-hydroxy cyclohexyl, and R³ is phenyl, any of which can be optionally substituted.

In another embodiment, the MerTK inhibitors useful in treating a disorder described herein have the structure of Formula III:

wherein:

R¹¹ is —R¹⁵R¹⁶, where R¹⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R¹⁶ is hydrogen, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocycloalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, heteroarylalkyl, hydroxyl, alkoxy, haloalkoxy, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, or acyloxy, and wherein R¹⁶ is optionally substituted one, two, three, four or five times;

m=0, 1, 2 or 3;

R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, alkoxyalkyl, hydroxyalkyl or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times;

R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocylic ring that can be optionally substituted;

R¹³ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times;

or R¹² and R¹³ together form a linking group;

R⁴ is H, loweralkyl, halo, or loweralkoxy;

R⁹ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times (typically R⁹ is H);

R¹¹ and R¹⁴ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted;

R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted;

R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl;

R¹⁴ is hydrogen, alkyl or alkylaryl;

with the proviso:

wherein if R⁹ and R¹³ with the nitrogen to which they are bonded do not form a heterocyclic group then one of R⁹ or R¹³ is hydrogen; and

wherein if R¹⁰ and R¹² with the nitrogen to which they are bonded do not form a heterocyclic group then one of R¹⁰ or R¹² is hydrogen; and

wherein if R¹² and R¹³ together form a linking group, then both R⁹ and R¹³ are hydrogen;

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cycloalkyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cyclohexyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is para-hydroxy cyclohexyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein is heteroaryl, R¹² is cycloalkyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cyclohexyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is para-hydroxy cyclohexyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cycloalkyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cyclohexyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is para-hydroxy cyclohexyl, R¹³ is loweralkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cycloalkyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cyclohexyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is para-hydroxy cyclohexyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cycloalkyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cyclohexyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is para-hydroxy cyclohexyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cycloalkyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cyclohexyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein is phenyl, R¹² is para-hydroxy cyclohexyl, R¹³ is butyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein is aryl, R¹² is cycloalkyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cyclohexyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is para-hydroxy cyclohexyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cycloalkyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cyclohexyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is para-hydroxy cyclohexyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cycloalkyl, R¹³ is cycloalkylalkyl R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cyclohexyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is para-hydroxy cyclohexyl, R¹³ is cycloalkylalkyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cycloalkyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is and aryl R¹² is cyclohexyl, R¹³ is aryl, R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein is aryl, R¹² is para-hydroxy cyclohexyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cycloalkyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, and R¹² is cyclohexyl, R¹³ is aryl, R⁴, R⁹, R¹⁰, are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is para-hydroxy cyclohexyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cycloalkyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is cyclohexyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is phenyl, R¹² is para-hydroxy cyclohexyl, R¹³ is aryl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cycloalkyl, R¹³ is phenyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is aryl, R¹² is cyclohexyl, R¹³ is phenyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein is aryl, R¹² is para-hydroxy cyclohexyl, R¹³ is phenyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cycloalkyl, R¹³ is phenyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is cyclohexyl, R¹³ is phenyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In some embodiments, structures are provided including Formula III, wherein R¹¹ is heteroaryl, R¹² is para-hydroxy cyclohexyl, R¹³ is phenyl, and R⁴, R⁹, R¹⁰, and R¹⁴ are H or loweralkyl, any of which can be optionally substituted.

In another embodiment, the MerTK inhibitors useful in treating a disorder described herein have the structure of Formula IV:

wherein:

ring A is a 5- or 6-membered heteroaryl group (for example, pyridyl, pyrimidyl, thiazol, furanyl, pyridazinyl, pyrazinyl, imidazol, etc.). The dashed lines are optional double bonds. X is N or O. Y is a carbon atom or an S or N heteroatom in ring A in any suitable location.

R¹⁹ is —R²⁰R²¹, where R²⁰ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R²¹ is hydrogen, alkyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocyclolalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, alkylheteroaryl, halo, hydroxyl, alkoxy, haloalkoxy, mercapto, alkyl-S(O)_(m)—, haloalkyl-S(O)_(m)—, alkenyl-S(O)_(m)—, alkynyl-S(O)_(m)—, cycloalkyl-S(O)_(m)—, cycloalkylalkyl-S(O)_(m)—, aryl-S(O)_(m)—, arylalkyl-S(O)_(m)—, heterocyclo-S(O)_(m)—, heterocycloalkyl-S(O)_(m)—, amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, acylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstitutedamino, acylamino, acyloxy, ester, amide, COOH, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, and wherein R²¹ is optionally substituted one, two or three times; or

two adjacent R¹⁹ groups can form an aryl or heteroaryl ring with the carbons that they are bonded to and can be optionally substituted;

R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl hydroxyalkyl, alkoxyalkyl, or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times;

R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocylic ring that can be optionally substituted;

R¹³ is selected from the group consisting of H, alkyl, hydroxyalkyl, aryl, arylalkyl; cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times;

or R¹² and R¹³ together form a linking group;

R⁴ is H, loweralkyl, halo, or loweralkoxy;

R⁹ is selected from the group consisting of H, alkyl, aryl, arylalkyl; cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times (typically R⁹ is H); or

R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted;

R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl;

m=0, 1, 2 or 3;

p=0, 1 or 2;

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

Particular examples of the foregoing include, but are not limited to:

wherein p=0, 1, or 2.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cycloalkyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cyclohexyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cycloalkyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cyclohexyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, R¹² is cycloalkyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cyclohexyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is loweralkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cycloalkyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cyclohexyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cycloalkyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cyclohexyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cycloalkyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cyclohexyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is butyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cycloalkyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cyclohexyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cycloalkyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cyclohexyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cycloalkyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cyclohexyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is cycloalkylalkyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cycloalkyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cyclohexyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cycloalkyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cyclohexyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cycloalkyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is cyclohexyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is aryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is aryl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cycloalkyl, R¹³ is phenyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is cyclohexyl, R¹³ is phenyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heterocycloalkyl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is phenyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cycloalkyl, R¹³ is phenyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is cyclohexyl, R¹³ is phenyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, structures are provided including Formulas IVa and IVb, wherein R¹⁹ is heteroaryl, p=1, R¹² is para-hydroxy cyclohexyl, R¹³ is phenyl, and R⁹ and R¹⁰ are H, any of which can be optionally substituted.

In some embodiments, R⁶ is heterocyclo or hydrogen.

In some embodiments, R⁶ is alkylheterocycloalkyl.

In some embodiments, R¹⁶ is heterocyclo or hydrogen.

In some embodiments, R²¹ is heterocyclo or hydrogen.

In some embodiments, R¹⁶ is alkylheterocycloalkyl.

In some embodiments, R²¹ is alkylheterocycloalkyl.

In some embodiments, the heterocycloalkyl group is appended to the parent molecular moiety through an alkyl group.

In another embodiment, the heterocycloalkyl group is appended to the parent molecular moiety through any carbon atom of the alkyl group.

In some embodiments, the heterocycloalkyl group is appended to the parent molecular moiety through the heterocyclo group.

In some embodiments, R³ is heterocyclo.

In some embodiments, R¹³ is heterocyclo.

In some embodiments, R³ is alkyl.

In some embodiments, R¹³ is alkyl.

In some embodiments, R³ is cycloalkyl.

In some embodiments, R¹³ is cycloalkyl.

In some embodiments, R³ is cycloalkylalkyl.

In some embodiments, R¹³ is cycloalkylalkyl.

In some embodiments, R² is cycloalkyl.

In some embodiments, R¹² is cycloalkyl.

In some embodiments, R² is para-hydroxy cyclohexyl.

In some embodiments, R¹² is para-hydroxy cyclohexyl.

In some embodiments, one of R⁹ or R¹³ can be hydrogen.

In some embodiments, one of R¹⁰ or R¹² can be hydrogen.

In another aspect, new pyrimidine compounds having the uses described herein have a structure selected from the compounds of Table 1, or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof

TABLE 1 NONLIMITING EXAMPLES OF NOVEL PYRIMIDINE COMPOUNDS Structure Compound_ID

UNC4171A

UNC4198A

UNC3231A

UNC1852A

UNC3209A

UNC2902A

UNC4332A

UNC4234A

UNC4235A

UNC4236A

UNC4238A

UNC4239A

UNC4246A

UNC4254A

UNC4255A

UNC4256A

UNC4260A

UNC4274A

UNC4286A

UNC4285A

UNC4287A

UNC4288A

UNC4289A

UNC4290A

UNC4302A

UNC4303A

UNC4304A

UNC4307A

UNC4344A

UNC4103A

UNC4104A

UNC4161A

UNC4162A

UNC4163A

UNC4165A

UNC4197A

UNC3668A

UNC4223A

UNC4261A

UNC4268A

UNC4269A

UNC4270A

UNC4272A

UNC4322A

UNC4323A

UNC4333A

UNC4353A

UNC3664A

UNC3665A

UNC3666A

UNC3667A

UNC3669A

UNC4359A

UNC3022A

UNC3051A

UNC3053A

UNC3052A

UNC4240A

UNC4241A

UNC4242A

UNC4243A

UNC4244A

UNC4247A

UNC4372A

UNC4373A

UNC4377A

UNC4397A

UNC4398A

UNC4105A

UNC4106A

UNC4109A

UNC4110A

UNC4111A

UNC4112A

UNC4113A

UNC4160A

UNC4166A

UNC4167A

UNC4168A

UNC4196A

UNC4169A

UNC4220A

UNC4221A

UNC4279A

UNC4281A

UNC4222A

UNC4230A

UNC4335A

UNC4336A

UNC4338A

UNC4339A

UNC4354A

UNC4356A

UNC4358A

UNC4387A

UNC4337A

UNC4409A

UNC4410A

UNC4411A

UNC4340A

UNC4386A

UNC4352A

UNC4378A

In another aspect, provided herein are novel, improved pyrimidine compounds useful as anti-thrombotic or anti-clotting agents, anti-infective agents, anti-cancer agents, and/or immunomodulatory agents having a structure selected from Formula IVe, IVf, IVg, and IVh:

wherein:

R²² is —R²³R²⁴, where R²³ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R²⁴ is alkyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocyclolalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, alkylheteroaryl, halo, hydroxyl, alkoxy, haloalkoxy, mercapto, alkyl-S(O)_(m)—, haloalkyl-S(O)_(m)—, alkenyl-S(O)_(m)—, alkynyl-S(O)_(m)—, cycloalkyl-S(O)_(m)—, cycloalkylalkyl-S(O)_(m)—, aryl-S(O)_(m)—, arylalkyl-S(O)_(m)—, heterocyclo-S(O)_(m)—, heterocycloalkyl-S(O)_(m)—, amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstitutedamino, acylamino, acyloxy, ester, amide, COOH, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, and wherein R²⁴ is optionally substituted one, two or three times;

wherein R⁹, R¹⁰, R¹², and R¹³ are as defined above;

and pharmaceutically acceptable salts thereof.

Particular examples of Formula IVe, IVf, IVg, and IVh include, but are not limited to, the following:

or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof.

Specific examples of linking groups include, but are not limited to:

where each n and m is independently 0, 1, 2, 4, 5, or 6; and where each of the linking group structures illustrated above may optionally be substituted, e.g., substituted one, two, or three times with independently selected polar groups.

The active compounds disclosed herein can, as noted above, be provided in the form of their pharmaceutically acceptable salts. Pharmaceutically acceptable salts are salts that retain the desired biological activity of the parent compound and do not impart undesired toxicological effects. Nonlimiting examples of such salts are (a) acid addition salts formed with inorganic acids, for example hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; and salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, and the like; (b) salts formed from elemental anions such as chlorine, bromine, and iodine, and (c) salts derived from bases, such as ammonium salts, alkali metal salts such as those of sodium and potassium, alkaline earth metal salts such as those of calcium and magnesium, and salts with organic bases such as dicyclohexylamine and N-methyl-D-glucamine.

Active compounds as described herein can be prepared in accordance with known procedures, or variations thereof that will be apparent to those skilled in the art.

3. Pharmaceutical Compositions and Dosages for all Indications

The active compounds described above may be formulated for administration in a pharmaceutical carrier in accordance with known techniques. See, e.g., Remington, The Science And Practice of Pharmacy (9^(th) Ed. 1995). In the manufacture of a pharmaceutical formulation according to the invention, the active compound (including the physiologically acceptable salts thereof) is typically admixed with, inter alia, an acceptable carrier. The carrier must, of course, be acceptable in the sense of being compatible with any other ingredients in the formulation and must not be deleterious to the patient. The carrier may be a solid or a liquid, or both, and is preferably formulated with the compound as a unit-dose formulation, for example, a tablet, which may contain from 0.01 or 0.5% to 95% or 99% by weight of the active compound. One or more active compounds may be incorporated in the formulations of the invention, which may be prepared by any of the well-known techniques of pharmacy comprising admixing the components, optionally including one or more accessory ingredients.

In one aspect, the invention provides a pharmaceutical composition comprising a pharmaceutically effective amount of an active compound as described herein and a pharmaceutically acceptable carrier.

The compounds provided herein are administered for medical therapy in a therapeutically effective amount. The amount of the compounds administered will typically be determined by a physician, in the light of the relevant circumstances, including the condition to be treated, the chosen route of administration, the compound administered, the age, weight, and response of the individual patient, the severity of the patient's symptoms, and the like.

The formulations of the invention include those suitable for oral, rectal, topical, buccal (e.g., sub-lingual), vaginal, parenteral (e.g., subcutaneous, intramuscular, intradermal, or intravenous), topical (i.e., both skin and mucosal surfaces, including airway surfaces), transdermal administration, and intraventricular injection (injection into a ventricle of the brain, e.g., by an implanted catheter or omman reservoir, such as in the case of morbid obesity), ocular (via injection, implantation or by reservoir), and intranasal, although the most suitable route in any given case will depend on the nature and severity of the condition being treated and on the nature of the particular active compound which is being used.

The compositions for oral administration can take the form of bulk liquid solutions or suspensions, or bulk powders. Typically, the compositions are presented in unit dosage forms to facilitate accurate dosing. The term “unit dosage forms” refers to physically discrete units suitable as unitary dosages for human subjects and other mammals, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect, in association with a suitable pharmaceutical excipient. Typical unit dosage forms include prefilled, premeasured ampules or syringes of the liquid compositions or pills, tablets, capsules or the like in the case of solid compositions. In such compositions, the compound is usually a minor component (as a nonlimiting example, from about 0.1 to about 50% by weight or preferably from about 1 to about 40% by weight) with the remainder being various vehicles or carriers and processing aids helpful for forming the desired dosing form. In one embodiment, the compound is present from about 1% to about 10% by weight.

Liquid forms suitable for oral administration may include a suitable aqueous or nonaqueous vehicle with buffers, suspending and dispensing agents, colorants, flavors and the like. Solid forms may include, for example, any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.

Formulations suitable for oral administration may be presented in discrete units, such as capsules, cachets, lozenges, or tablets, each containing a predetermined amount of the active compound; as a powder or granules; as a solution or a suspension in an aqueous or non-aqueous liquid; or as an oil-in-water or water-in-oil emulsion. Such formulations may be prepared by any suitable method of pharmacy which includes the step of bringing into association the active compound and a suitable carrier (which may contain one or more accessory ingredients as noted above). In general, the formulations of the invention are prepared by uniformly and intimately admixing the active compound with a liquid or finely divided solid carrier, or both, and then, if necessary, shaping the resulting mixture. For example, a tablet may be prepared by compressing or molding a powder or granules containing the active compound, optionally with one or more accessory ingredients. Compressed tablets may be prepared by compressing, in a suitable machine, the compound in a free-flowing form, such as a powder or granules optionally mixed with a binder, lubricant, inert diluent, and/or surface active/dispersing agent(s). Molded tablets may be made by molding, in a suitable machine, the powdered compound moistened with an inert liquid binder. In one embodiment, the compounds are administered in a controlled release formulation.

Formulations suitable for buccal (sub-lingual) administration include lozenges comprising the active compound in a flavored base, usually sucrose and acacia or tragacanth; and pastilles comprising the compound in an inert base such as gelatin and glycerin or sucrose and acacia.

Formulations of the present invention suitable for parenteral administration comprise sterile aqueous and non-aqueous injection solutions of the active compound, which preparations are preferably isotonic with the blood of the intended recipient. These preparations may contain anti-oxidants, buffers, bacteriostats and solutes which render the formulation isotonic with the blood of the intended recipient. Aqueous and non-aqueous sterile suspensions may include suspending agents and thickening agents. The formulations may be presented in unit\dose or multi-dose containers, for example sealed ampoules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, saline or water-for-injection immediately prior to use. Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described. For example, in one aspect of the present invention, there is provided an injectable, stable, sterile composition comprising a compound of Formula (I), or a salt thereof, in a unit dosage form in a sealed container. The compound or salt is provided in the form of a lyophilizate which is capable of being reconstituted with a suitable pharmaceutically acceptable carrier to form a liquid composition suitable for injection thereof into a subject. The unit dosage form typically comprises from about 10 mg to about 10 grams of the compound or salt. When the compound or salt is substantially water-insoluble, a sufficient amount of emulsifying agent which is physiologically acceptable may be employed in sufficient quantity to emulsify the compound or salt in an aqueous carrier. One such useful emulsifying agent is phosphatidyl choline.

Injectable compositions are typically based upon injectable sterile saline or phosphate-buffered saline or other injectable carriers known in the art.

Formulations suitable for rectal administration are preferably presented as unit dose suppositories. These may be prepared by admixing the active compound with one or more conventional solid carriers, for example, cocoa butter, and then shaping the resulting mixture.

Formulations suitable for topical application to the skin preferably take the form of an ointment, cream, lotion, paste, gel, spray, aerosol, or oil. Carriers which may be used include petroleum jelly, lanoline, polyethylene glycols, alcohols, transdermal enhancers, and combinations of two or more thereof.

Formulations suitable for transdermal administration may be presented as discrete patches adapted to remain in intimate contact with the epidermis of the recipient for a prolonged period of time. Formulations suitable for transdermal administration may also be delivered by iontophoresis (see, for example, Pharmaceutical Research 3 (6):318 (1986)) and typically take the form of an optionally buffered aqueous solution of the active compound. Suitable formulations comprise citrate or bis\tris buffer (pH 6) or ethanol/water and contain from 0.1 to 0.2M active ingredient.

Further, the present invention provides liposomal formulations of the compounds disclosed herein and salts thereof. The technology for forming liposomal suspensions is well known in the art. When the compound or salt thereof is an aqueous-soluble salt, using conventional liposome technology, the same may be incorporated into lipid vesicles. In such an instance, due to the water solubility of the compound or salt, the compound or salt will be substantially entrained within the hydrophilic center or core of the liposomes. The lipid layer employed may be of any conventional composition and may either contain cholesterol or may be cholesterol-free. When the compound or salt of interest is water-insoluble, again employing conventional liposome formation technology, the salt may be substantially entrained within the hydrophobic lipid bilayer which forms the structure of the liposome. In either instance, the liposomes which are produced may be reduced in size, as through the use of standard sonication and homogenization techniques.

Of course, the liposomal formulations containing the compounds disclosed herein or salts thereof, may be lyophilized to produce a lyophilizate which may be reconstituted with a pharmaceutically acceptable carrier, such as water, to regenerate a liposomal suspension.

Other pharmaceutical compositions may be prepared from the water-insoluble compounds disclosed herein, or salts thereof, such as aqueous base emulsions. In such an instance, the composition will contain a sufficient amount of pharmaceutically acceptable emulsifying agent to emulsify the desired amount of the compound or salt thereof. Particularly useful emulsifying agents include phosphatidyl cholines, and lecithin.

In addition to compounds of Formula I, II, III, or IV, or other active compounds described herein, or their salts, the pharmaceutical compositions may contain other additives, such as pH-adjusting additives. In particular, useful pH-adjusting agents include acids, such as hydrochloric acid, bases or buffers, such as sodium lactate, sodium acetate, sodium phosphate, sodium citrate, sodium borate, or sodium gluconate. Further, the compositions may contain microbial preservatives. Useful microbial preservatives include methylparaben, propylparaben, and benzyl alcohol. The microbial preservative is typically employed when the formulation is placed in a vial designed for multidose use. Of course, as indicated, the pharmaceutical compositions of the present invention may be lyophilized using techniques well known in the art.

The Mer TKI compound of this invention can also be administered in sustained release forms or from sustained release drug delivery systems. A description of representative sustained release materials can be found in Remington's Pharmaceutical Sciences.

In certain embodiments, the formulation comprises water. In another embodiment, the formulation comprises a cyclodextrin derivative. In certain embodiments, the formulation comprises hexapropyl-β-cyclodextrin. In a more particular embodiment, the formulation comprises hexapropyl-β-cyclodextrin (10-50% in water).

The present invention also includes pharmaceutically acceptable acid addition salts of compounds of the compounds of the invention. The acids which are used to prepare the pharmaceutically acceptable salts are those which form non-toxic acid addition salts, i.e. salts containing pharmacologically acceptable anions such as the hydrochloride, hydroiodide, hydrobromide, nitrate, sulfate, bisulfate, phosphate, acetate, lactate, citrate, tartrate, succinate, maleate, fumarate, benzoate, para-toluenesulfonate, and the like.

The above-described components for pharmaceutical compositions are merely representative. Other materials as well as processing techniques and the like are set forth in Part 8 of Remington's Pharmaceutical Sciences, 17th edition, 1985, Mack Publishing Company, Easton, Pa., which is incorporated herein by reference.

As noted above, the present invention provides pharmaceutical formulations comprising the active compounds (including the pharmaceutically acceptable salts thereof), in pharmaceutically acceptable carriers for oral, rectal, topical, buccal, parenteral, intramuscular, intradermal, or intravenous, and transdermal administration.

The therapeutically effective dosage of any specific compound, the use of which is in the scope of present invention, will vary somewhat from compound to compound, and patient to patient, and will depend upon the condition of the patient and the route of delivery. As a general proposition, a dosage from about 0.1 to about 50 mg/kg will have therapeutic efficacy, with all weights being calculated based upon the weight of the active compound, including the cases where a salt is employed. Toxicity concerns at the higher level may restrict intravenous dosages to a lower level such as up to about 10 mg/kg, with all weights being calculated based upon the weight of the active base, including the cases where a salt is employed. The duration of the treatment can be once per day for a period of two to three weeks or until the condition is essentially controlled.

The therapeutically effective dosage of any active compound described herein will be determined by the health care practitioner depending on the condition, size and age of the patient as well as the route of delivery. In one non-limited embodiment, a dosage from about 0.1 to about 200 mg/kg has therapeutic efficacy, with all weights being calculated based upon the weight of the active compound, including the cases where a salt is employed. In some embodiments, the dosage can be the amount of compound needed to provide a serum concentration of the active compound of up to between about 1 and 5, 10, 20, 30, or 40 μM. In some embodiments, a dosage from about 10 mg/kg to about 50 mg/kg can be employed for oral administration. Typically, a dosage from about 0.5 mg/kg to 5 mg/kg can be employed for intramuscular injection. In some embodiments, dosages can be from about 1 μmol/kg to about 50 μmol/kg, or, optionally, between about 22 μmol/kg and about 33 μmol/kg of the compound for intravenous or oral administration. An oral dosage form can include any appropriate amount of active material, including for example from 5 mg to, 50, 100, 200, or 500 mg per tablet or other solid dosage form.

Active compounds may be administered as pharmaceutically acceptable prodrugs, which are those prodrugs of the active compounds of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like, commensurate with a reasonable risk/benefit ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention. The term “prodrug” refers to compounds that are transformed, sometimes rapidly in vivo to yield the parent compound of the above formulae, for example, by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, Prodrugs as Novel delivery Systems, Vol. 14 of the A.C.S. Symposium Series and in Edward B. Roche, ed., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated by reference herein. See also U.S. Pat. No. 6,680,299 Examples include a prodrug that is metabolized in vivo by a subject to an active drug having an activity of active compounds as described herein, wherein the prodrug is an ester of an alcohol or carboxylic acid group, if such a group is present in the compound; an acetal or ketal of an alcohol group, if such a group is present in the compound; an N-Mannich base or an imine of an amine group, if such a group is present in the compound; or a Schiff base, oxime, acetal, enol ester, oxazolidine, or thiazolidine of a carbonyl group, if such a group is present in the compound, such as described in U.S. Pat. No. 6,680,324 and U.S. Pat. No. 6,680,322.

In one aspect of the invention, a method is provided to treat a host by administering a daily amount of a Mer TKI including active compounds of the present invention, which may be provided in dosages once or more a day. In one embodiment, the Mer TKI dose is between about 0.5 mg and about 200 mg. In one embodiment, the dose is at least about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 10 mg, about 12 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, about 100 mg, about 110 mg, about 125 mg, about 140 mg, about 150, about 175, or about 200 mg. In another embodiment, the dose is between about 200 mg and 1250 mg. In one embodiment, the dose is about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg or more.

In one embodiment, the compounds described herein are combined with an additional anti-tumor agent, anti-neoplastic agent, anti-cancer agent, immunomodulatory agent, immunostimulatory agent, anti-infective agents, anti-thrombotic, and/or anti-clotting agent. The dosage administered to the host can be similar to that as administered during monotherapy treatment, or may be lower, for example, between about 0.5 mg and about 150 mg. In one embodiment, the dose is at least about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 10 mg, about 12 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, about 100 mg, about 110 mg, about 125 mg, about 140 mg, or about 150 mg.

In one embodiment, for the case of the co-administration of an active compound in combination with an additional anti-tumor agent, anti-neoplastic agent, anti-cancer agent, immunomodulatory agent, immunostimulatory agent, anti-infective agents, anti-thrombotic, and/or anti-clotting agent, as otherwise described herein, the amount of the compound according to the present invention to be administered ranges from about 0.01 mg/kg of the patient to about 50 mg/kg or more of the patient or considerably more, depending upon the second compound to be co-administered, the condition of the patient, severity of the disease to be treated, and the route of administration. In one embodiment, the additional anti-tumor agent, anti-neoplastic agent, anti-cancer agent, immunomodulatory agent, immunostimulatory agent, anti-infective agents, anti-thrombotic, and/or anti-clotting agent may, for example, be administered in amounts ranging from about 0.01 mg/kg to about 500 mg/kg. In one embodiment, for oral dosing, suitable daily dosages are, for example, between about 0.1-4000 mg administered orally once-daily, twice-daily, or three times-daily, continuous (every day) or intermittently (e.g., 3-5 days a week).

Methods of Use of the Active Compounds 4. Anti-Infective Agents

It has been discovered that an effective amount of the pyrimidinyl compounds described in Formulas I, II, III and IV below or as otherwise provided herein, can be administered as an immunomodulatory agent to stimulate the innate immune system. This immunostimulatory activity can be used therapeutically to treat a host with an infection. In one embodiment, the infection is a viral infection. In one embodiment, the infection is a bacterial infection. In an alternative embodiment, an effective amount of the pyrimidinyl compounds described in Formulas I, II, III and IV below or as otherwise provided herein can be used to treat a host bearing any virus-related infection where the virus has a virion envelope phosphatidyl serine that complexes with MerTK to achieve viral entry or is otherwise facilitated by MerTK in the infectious process or maintenance.

Viral Infections.

The virus may be an enveloped virus or a non-enveloped virus. In one embodiment, the host is infected or threatened to become infected with a virus selected from, for example, Flaviviridae viruses, including Flavivirus (such as Yellow Fever, West Nile and Dengue), Hepacivirus (Hepatitis C virus, “HCV”), Pegivirus and Pestivirus (Bovine viral diarrhea virus); Filoviridae viruses, including Ebola viruses; Togaviridae viruses, including Chikungunya virus; Coronaviruses, such as SARS (Severe acute respiratory syndrome) and MERS (Middle East respiratory syndrome); Orthomyxoviridae viruses, for example influenza; Paramyxoviridae viruses, for example Respiratory syncytial virus (RSV), measles and mumps; and Caliciviridae viruses, including Lagovirus, Vesivirus, and Sapovirus and Norovirus (Norwalk-like virus), and Lentiviruses, for example, HIV. In one embodiment, an active compound disclosed herein is administered in combination or alternation with another anti-viral agent for combination therapy. In one embodiment, the compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

More broadly, the host to be treated may be infected with an enveloped virus including, but not limited to, viruses of the following families: Bornaviridae, Bunyaviridae, Coronaviridae, Filoviridae, Flaviridae, Hepadnaviridae, Herpesviridae, Nyamiviridae, Orthomyxoviridae, Paramyxoviridae, Poxyiridae, Retroviridae, Rhabdoviridae, and Togaviridae. Examples of viruses form the Bunyaviridae family include, but are not limited to, bunya viruses such as La Crosse virus and Hantaan. Examples of viruses from the Coronaviridae family include, but are not limited to, coronaviruses such as SARS virus or Toroviruses. Examples of viruses from the Filoviradae family include, but are not limited to, Ebola and Marburg. Examples of viruses from the Flaviridae family include, but are not limited to, dengue, encephalitis viruses including West Nile virus, Japanese encephalitis virus and yellow fever virus and Hepatitis C virus. Examples of viruses from the Hepadnaviridae family include, but are not limited to, Hepatitis B. Examples of viruses from the Herpesviridae family include, but are not limited to, cytomegalovirus, herpes simplex viruses 1 and 2, HHV-6, HHV-7, HHV-8, pseudorabies virus, and varicella zoster virus. Examples of viruses from the Orthomyxoviridae family include, but are not limited to, influenza virus. Examples of viruses from the Paramyxoviridae family include, but are not limited to, measles, metapneumovirus, mumps, parainfluenza, respiratory syncytial virus, and sendai. Examples of viruses from the Poxviridae family include, but are not limited to, pox viruses such as smallpox, monkey pox, and Molluscum contagiosum virus, variola viruses, vaccinia virus, and yatapox viruses such as Tanapox and Yabapox. Examples of viruses from the Retroviridae family include, but are not limited to, Coltiviruses such as CTFV and Banna virus, human immunodeficiency viruses such as HIV-1 and HIV-2, murine leukemia virus, simian immunodeficiency virus, feline immunodeficiency virus, human T-cell leukemia viruses 1 and 2, and XMRV. Examples of viruses from the Rhabdoviridae family include, but are not limited to, vesicular stomatitis and rabies. Examples of viruses from the Togaviridae family include, but are not limited to, rubella viruses or alpha viruses such as Chikungunya virus, Eastern equine encephalitis virus, O'nyong'nyong virus, Ross River virus, Semliki Forest virus, Sindbis, Venezuelan equine encephalitis or Western equine encephalitis virus.

In one embodiment, the host is infected with Chikungunya virus. In one embodiment, the host is infected with Ebola virus. In one embodiment, an active compound or Mer TKI as described herein is used in combination with brincidofovir (CMX001).

In another particular embodiment, the host is infected with a non-enveloped virus, sch as, but not limited to, viruses of the following families: Adenoviridae, Arenaviridae, Birnaviridae, Calciviridae, Iridoviridae, Ophioviridae Parvoviradae, Papillomaviridae, Papovaviridae, Picornaviridae, and Reoviridae. Examples of viruses from the Adenoviridae family include, but are not limited to adenoviruses. Examples of viruses from the Arenaviradae family include, but are not limited to, hemorrhagic fever viruses such as Guanarito, LCMV, Lassa, Junin, and Machupo. Examples of viruses from the Iridoviridae family include, but are not limited to, African swine fever virus. Examples of viruses from the Papillomavirus family include, but are not limited to, papillomaviruses. Examples of viruses from the Papovaviridae family include, but are not limited to, polyoma viruses such as BK virus and JC virus. Examples of viruses from the Parvoviridae family include, but are not limited to, parvoviruses such as human bocavirus and adeno-associated virus. Examples of viruses from the Picornaviridae family include, but are not limited to, aptoviruses, cardioviruses, coxsackieviruses, echoviruses, enteric viruses, enteroviruses, foot and mouth disease virus, hepatitis A virus, hepatoviruses, Poliovirus, and rhinovirus. Examples of viruses from the Reoviradae family include, but are not limited to, orbiviruses, reoviruses and rotaviruses.

In another embodiment, a host is infected with a virus such as an astroviruses, caliciviruses including but not limited to, Norovirus and Norwalk, and Hepeviruses including, but not limited to, Hepatitis E.

As described above, a compound described herein can be administered to a host suffering from a viral infection in combination with another anti-viral or anti-infective compound. Antiviral compounds that can be used in combination with the compounds described herein include, but are not limited to, abacavir, acyclovir, adefovir, amantadine, amprenavir, ampligen, arbitol, atazanavir, balavir, boceprevir, boceprevirertet, cidofovir, dolutegravir, darunavir, delavirdine, didanosine, docosanol, edoxudine, efavirenz, emtricitabine, epivir, enfuvirtide, entecavir, famciclovir, fomivirsen, fosamprenavir, foscarnet, fosfonet, ganciclovir, ibacitabine, imunovir, idoxuridine, imiquimod, indinavir, lamivudine, lopinavir, loviride, maraviroc, moroxydine, nelfinavir, nevirapine, nexavir, oseltamivir, penciclovir, peramivir, pleconaril, podophyllotoxin, raltegravir, ribavirin, rilpivirine, rimantadine, pyramidine, saquinavir, simeprevir, sofosbuvir, stavudine, telaprevir, tenofovir, tipranavir, trifluridine, trizivir, tromantadine, traporved, truvada, valaciclovir, valganciclovir, vicriviroc, vidarabine, viramidine, zalcitabine, zanamivir, and zidovudine.

In one embodiment, a host is infected with a human immunodeficiency virus and is administered a compound described herein in combination with the anti-HIV combination drug, such as Atripla® or other drug that includes emtricitabine. In another embodiment, the patient with the human immunodeficiency virus can be treated with atazanavir, ritonavir, or Truvada® in combination with a compound described herein. In another embodiment, the patient infected with human immunodeficiency virus can be treated with the combination of dolutegravir, Truvada® and a compound described herein. In another embodiment, human immunodeficiency virus can be treated with the combination dolutegravir, Epzicom® and a compound described herein. In another embodiment, a host infected with human immunodeficiency virus can be treated with a combination of raltegravir, Truvada® and a compound described herein. In another embodiment, a host infected with human immunodeficiency virus can be treated with the combination of Complera® and a compound described herein. It will be appreciated by one skilled in the art that a host infected with HIV can be treated with a number of combinations of drugs depending on the mutation pattern of the virus. The patient can be treated with an appropriate combination of drugs in combination with a compound described herein.

In one embodiment, the host is infected with a hepatitis C virus and is treated with an anti-hepatitis C drug in addition to the active compound described herein. For example, the patient can be treated with a combination of Sovaldi™, Harvoni®, ribavirin, and/or a pegylated interferon and a compound described herein. In one embodiment the pegylated interferon is PegInton®. In another embodiment, the pegylated interferon is Pegasys®. In one embodiment, the host infected with hepatitis C virus is treated with Sovaldi™, ribavirin and a compound described herein. In one embodiment, the host infected with hepatitis C virus is treated with Harvoni®, ribavirin and a compound described herein. In one embodiment, a host infected with hepatitis C virus is treated with a combination of Olysio™, ribavirin, a pegylated interferon and a compound described herein. In one embodiment the pegylated interferon is Peglntron®. In another embodiment, the pegylated interferon is Pegasys®. In one embodiment, the host is infected with a hepatitis C virus and is treated with a combination of ABT-267, ABT-333 and ABT-450/ritonavir, in addition to an active compound described herein. In one embodiment, the host is infected with a hepatitis C virus and is treated with a combination of MK-5172 and MK-8742, in addition to an active compound described herein.

In one embodiment, a host infected with hepatitis C genotype 1 is treated with a combination of Sovaldi™, ribavirin, a pegylated interferon and a compound described herein for 12 weeks. In another embodiment, a host infected with hepatitis C genotype 1 is treated with Sovaldi™ and a compound described herein for 12 weeks followed by ribavirin, pegylated interferon and a compound described herein for 24 weeks. In one embodiment, a host infected with hepatitis C genotype 2 is treated with Sovaldi™, ribavirin, and a compound described herein for 12 weeks. In one embodiment, a host infected with hepatitis C genotype 3 is treated with Sovaldi™, ribavirin, and a compound described herein for 24 weeks. In another embodiment, a host infected with hepatitis C genotype 3 is treated with Sovaldi™, ribavirin, pegylated interferon, and a compound described herein for 12 weeks. In one embodiment, a host infected with hepatitis C genotype 4 is treated with Sovaldi™, ribavirin, pegylated interferon, and a compound described herein for 12 weeks. In another embodiment, a host infected with hepatitis C genotype 4 is treated with a combination of Olysio™, and a compound described herein for 12 weeks followed by ribavirin, pegylated interferon and a compound described herein for 24-28 weeks.

In one embodiment, a host infected with hepatitis C genotype 5 is treated with Sovaldi™, ribavirin, pegylated interferon, and a compound described herein for 12 weeks. In one embodiment, a host infected with hepatitis C genotype 5 is treated with ribavirin, pegylated interferon, and a compound described herein for 48 weeks. In one embodiment, a host infected with hepatitis C genotype 6 is treated with Sovaldi™, ribavirin, pegylated interferon, and a compound described herein for 12 weeks. In one embodiment, a host infected with hepatitis C genotype 6 is treated with ribavirin, pegylated interferon, and a compound described herein for 48 weeks.

In one embodiment, a host infected with hepatitis C genotype 1 is treated with Sovaldi™, Olysio™, ribavirin, and a compound described herein for 12 weeks. In another embodiment, a host infected with hepatitis C genotype 1 is treated with Sovaldi™, ribavirin, and a compound described herein for 24 weeks. In one embodiment, a host infected with hepatitis C genotype 2 is treated with Sovaldi™, ribavirin, and a compound described herein for 12 weeks. In one embodiment, a host infected with hepatitis C genotype 3 is treated with Sovaldi™, ribavirin, and a compound described herein for 24 weeks. In one embodiment, a patient infected with hepatitis C genotype 4 is treated with Sovaldi™, ribavirin, and a compound described herein for 24 weeks.

In one embodiment, a host infected with papilloma virus is treated with imiquimod and a compound described herein. In another embodiment, a host infected with papilloma virus is treated with cryotherapy and a compound described herein. In another embodiment, papilloma virus is surgically removed from a host and the host is treated with a compound described herein. In one embodiment, the host receives a compound described herein prior to, during, and post-surgery. In one embodiment, the patient receives a compound described herein post-surgery.

In one embodiment a host infected with herpes simplex type 2 is treated with Famvir® and a compound described herein. In one embodiment a host infected with herpes simplex type 1 is treated with acyclovir and a compound described herein. In another embodiment, a host infected with herpes simplex type 2 is treated with acyclovir and a compound described herein. In one embodiment, a host infected with herpes simplex type 1 is treated with Valtrex® and a compound described herein. In another embodiment, a host infected with herpes simplex type 2 is treated with Valtrex® and a compound described herein. In one embodiment, a host infected with herpes simplex type 1 virus receives a compound described herein for 7 days prior to treatment with acyclovir. In one embodiment, a host infected with herpes simplex type 2 virus receives a compound described herein for 7 days prior to treatment with acyclovir. In one embodiment, a host infected with herpes simplex type 1 virus receives a compound described herein for 7 days prior to treatment with Valtrex®. In one embodiment, a host infected with herpes simplex type 2 virus receives a compound described herein for 7 days prior to treatment with Valtrex®.

In one embodiment a host infected with varicella zoster virus, VZV, is treated with acyclovir and a compound described herein. In another embodiment a host infected with varicella zoster virus, VZV, is treated with Valtrex® and a compound described herein. In one embodiment a host infected with varicella zoster virus, VZV, is treated with famciclovir and a compound described herein. In another embodiment a host infected with varicella zoster virus, VZV, is treated with foscarnet and a compound described herein. In one embodiment, a host infected with varicella zoster virus is treated with a compound described herein prior to vaccination with Zostavax®. In another embodiment, a host infected with varicella zoster virus is treated with a compound described herein prior to and post vaccination with Zostavax®.

In one embodiment a host infected with influenza virus is treated with Relenza® and a compound described herein. In another embodiment a host infected with influenza virus is treated with Tamiflu® and a compound described herein. In another embodiment a host is infected with influenza virus and is treated with amantadine and a compound described herein. In another embodiment, a host infected with influenza virus is treated with rimantadine and a compound described herein.

In one embodiment, a host infected with cytomegalovirus is treated with valganciclovir and a compound described herein. In another embodiment, a host infected with cytomegalovirus is treated with ganciclovir and a compound described herein. In one embodiment, a host infected with cytomegalovirus is treated with foscarnet and a compound described herein. In another embodiment, a host infected with cytomegalovirus is treated with cidofovir and a compound described herein.

In one embodiment, a host infected with hepatitis B virus is treated with lamivudine and a compound described herein. In another embodiment, a host infected with hepatitis B virus is treated with adefovir and a compound described herein.

In one embodiment, a host infected with hepatitis B virus is treated with tenofovir and a compound described herein. In another embodiment, a host infected with hepatitis B virus is treated with telbivudine and a compound described herein.

Bacterial Infections. In one embodiment of the present invention, a compound of Formula I, II, III, or IV, or other active compound described herein, is used in an effective amount to treat a host infected with a bacterial infection. In one embodiment, the bacteria treated is, for example, a Gram-negative bacilli (GNB), especially Escherichia coli, Gram-positive cocci (GPC), Staphylococcus aureus, Enterococcus faecalis, or Streptococcus pneumoniae. In one embodiment, the bacterial infection may be caused, for example, by a Gram-negative bacteria, including, but not limited to Escherichia coli, Salmonella, and other Enterobacteriaceae, Pseudomonas, Moraxella, Helicobacter, Stenotrophomonas, Bdellovibrio, acetic acid bacteria, Legionella, Staphylococcus aureus, Hemophilus influenzae, Klebsiella pneumoniae, Legionella pneumophila, Pseudomonas aeruginosa, Vibrio cholerae, Proteus mirabilis, Enterobacter cloacae, Serratia marcescens, Clostridium tetani, Helicobacter pylori, Salmonella enteritidis, Salmonella typhi, Shigella flexneri, or Acinetobacter baumanii. In one embodiment, the bacterial infection may be caused, for example, by a Gram-positive species from the following genera: Bacillus, Listeria, Staphylococcus, Enterococcus, Lactobacillus, Lactococcus, Leuconostoc, Pedicoccus, Streptococcus, Acetobacterium, Clostridium, Eubacterium, Heliobacterium, Heliospirillum, Megasphaera, Pectinatus, Selenomonas, Zymophilus, Sporomusa, Mycoplasma, Spiroplasma, Ureaplasma, or Erysipelothrix.

In one embodiment, the bacterial infection is associated with liver failure. In one embodiment, an active compound disclosed herein is administered in combination with an antibiotic or another anti-bacterial agent. In one embodiment, the compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, the bacterial infection is associated with liver failure. In one embodiment, an active compound disclosed herein is administered in combination with an antibiotic or another anti-bacterial agent. In one embodiment, the compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, a patient is suffering from acute-on-chronic liver failure (ACLF). In one embodiment, a patient is suffering from acute liver failure. In one embodiment, a patient is suffering from chronic liver failure. In one embodiment, the liver failure is caused by a disease or condition selected from alcoholic liver disease, chronic viral hepatitis type C, chronic viral hepatitis type B, chronic bile duct blockage, Wilson's disease, hemochromatosis, exposure to drug and toxins, autoimmune hepatitis, cystic fibrosis, alpha antitrypsin deficiency, obesity or schistosomiasis.

In one embodiment, an active compound disclosed herein is administered in combination with an antibiotic for the prevention or treatment of bacterial infections. Examples of antibiotics include, but are not limited to, cefotaxime (Claforan), ofloxacin (Floxin), norfloxacin (Noroxin) or trimethoprim/sulfamethoxazole (Bactrim, Septra).

5. Immunomodulatory and Immunostimulatory Agents

It has also been discovered that the compounds described herein can be used as immunomodulatory agents that reverse the MerTK-induced suppression of proinflammatory cytokines such as wound healing cytokines (IL-10 and GAS6) and enhance the expression of acute inflammatory cytokines (IL-12 and IL-6). In this way, the pyrimidine compounds can “re-normalize” or “re-program” the host microenvironment in the diseased tissue area to attack the diseased cells. This immunostimulatory activity can be used therapeutically to treat a host with a tumor, cancer or other neoplasm, or alternatively, to treat a host with an infection, for example, a viral or bacterial infection.

Taking advantage of the immunostimulatory activity of the compounds described herein, or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof, may be used for the treatment of a MERTK-negative (−/−) tumor or cancer. In one embodiment, the cancer is a MERTK-negative (−/−) breast cancer.

Therefore, as part of the invention, one or more of the compounds disclosed herein can be used as adjunctive therapy for its immunostimulatory effect as a means to increase the efficacy of the antineoplastic standard of care therapies, such as chemotherapeutic compounds or radiation.

In another aspect of the invention, one or more of the compounds disclosed herein can be used as adjunctive therapy for its immunostimulatory effect as a means to increase the efficacy of the antiviral or antibacterial standard of care therapies.

For example, a compound of Formula I, II, III, or IV, or another compound as described herein, is administered to a host in an immunomodulatory effective amount to inhibit Mer tyrosine kinase activity in the host's tumor associated macrophage to suppress tumor immunity. In one embodiment, the dosage of the Mer TKI administered as an immunomodulatory agent to stimulate innate anti-tumor immunity is lower than a dosage of a Mer TKI administered to a host as a direct anti-cancer agent. In one embodiment, the Mer TKI is administered at a dosage which exhibits immunomodulatory but not direct cytotoxic effect.

In one embodiment, the cancer is a MERTK-negative (−/−) cancer. In one embodiment, the MerTK inhibitory compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

Without wanting to be bound by any particular theory, it is believed that the administration of a chemotherapeutic agent results in the apoptosis of tumor cells, exposing antigenic tumor proteins. The host's innate immune system is thus stimulated to recognize the antigenic apoptotic components from the tumor cells after chemotherapy or ionizing radiation and mount an immune response. In one embodiment, the administration of a chemotherapeutic agent or ionizing radiation, before, with or subsequently followed by the administration of a Mer TKI is carried out using the normal standard of care chemotherapeutic protocol. In another embodiment, the standard of care protocol of the chemotherapeutic is changed in a manner that causes less toxicity to the host due to the adjunctive or synergistic activity of the Mer TKI.

In one embodiment, a method for the treatment of a tumor is provided that includes administering an effective amount of a Mer TKI to inhibit TK signaling in a tumor associated macrophage, without inhibiting the survival signal in the tumor itself. In this way, the Mer TKI can be used to ramp up the immune response to the tumor by inhibiting macrophage tumorogenic tolerance during normal tumor chemotherapeutic agent. The immunomodulatory dosage of the Mer TKI can be given prior to, with or after chemotherapeutic therapy and can be used simultaneously with or intermittently with the chemotherapeutic therapy. In one embodiment, less chemotherapeutic therapy is needed than the normal standard of care defined for that chemotherapeutic agent, due to the increased efficacy of the immune response in the surrounding tumor microenvironment. In one embodiment, a dose of Mer TKI including active compounds of the present invention (for example 0.5 to 150 mg/dose) is given as a type of adjunctive therapy with the chemotherapeutic agent.

In one aspect of the invention, a Mer TKI is administered to a host having a cancer as an immunomodulatory agent to inhibit Mer tyrosine kinase activity in a tumor associated macrophage in order to suppress tumor immunity. In one embodiment, the dosage of the Mer TKI administered as an immunomodulatory agent to stimulate innate anti-tumor immunity is lower than a dosage of a Mer TKI administered to a host as a direct anti-cancer agent. In one embodiment, the Mer TKI is administered at a dosage which exhibits immunomodulatory but not direct cytotoxic effects on the cancer.

In one embodiment, the dose associated with the immunomodulatory effect of an active compound of the present invention is about 2-fold, about 3-fold, about 4-fold, about 5-fold, about 6-fold, about 7-fold, about 8-fold, about 9-fold, about 10-fold or greater lower than the dose associated with a direct survival-signal inhibiting anti-tumor or cytotoxic effect, or the direct antiviral or antibacterial effect. In one embodiment, the dose used to induce an immunomodulatory effect in a host is between about 0.5 mg and about 150 mg. In one embodiment, the dose is about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 10 mg, about 12 mg, about 15 mg, about 20 mg, about 25 mg, about 30 mg, about 35 mg, about 40 mg, about 45 mg, about 50 mg, about 55 mg, about 60 mg, about 65 mg, about 70 mg, about 75 mg, about 80 mg, about 85 mg, about 90 mg, about 95 mg, about 100 mg, about 110 mg, about 125 mg, about 140 mg, or about 150 mg.

6. Anti-Tumor Agents, Including Anti-Cancer Agents

In one aspect of the invention, a compound of Formula I, II, III, or IV, or other active compound as described herein, is capable of direct anti-cancer effects by inhibiting Mer tyrosine kinase within tumor cells. In one embodiment, the cancer treated overexpresses MerTK. In one embodiment, the cancer which overexpresses MerTK is selected from the group consisting of acute myeloid leukemia, T-cell acute lymphoid leukemia, B-cell acute lymphoid leukemia, lung cancer, glioma, melanoma, prostate cancer, schwannoma, mantle cell lymphoma, and rhabdomyosarcoma. In an alternative embodiment, the cancer ectopically expresses MerTK. In one embodiment, the compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, the cancer treated has a mutation in the amino acid sequence of the MerTK extracellular or transmembrane domain selected from P40S (melanoma), S159F (lung), E204K (urinary tract) S428G (gastric), I431F (lung), A446G (kidney), N454S (liver), W485S/C (lymphoma), and V486I (melanoma). In one embodiment the cancer treated has a mutation in the amino acid sequence of the MerTK cytosolic domain mutation selected from L586F (urinary tract), G594R (breast), S626C (urinary tract), P672S (lung), L688M (colon), A708S (head and neck), N718Y (lung), R722stop (colon), M790V (lung), P802S (melanoma), V873I (liver), S905F (lung), K923R (melanoma), P958L (kidney), D983N (liver), and D990N (colon). In one embodiment, the compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment of the invention, a compound of Formula I, II, III, or IV, as described herein, is administered to a host with a cancer in combination with one or more additional chemotherapeutic agents, resulting in a synergistic anti-cancer effect and the prolonged survival of a host compared to treatment with either a compound described herein or chemotherapeutic agent alone. In one embodiment, the use of a MerTKI compound described herein in combination with a chemotherapeutic agent provides for increased anti-tumor effects without an increase in the standard of care dosage of the chemotherapeutic agent. In one embodiment, the use of a MerTKI compound described herein in combination with a chemotherapeutic provides for equivalent or increased anti-tumor effects utilizing a lower dosage of a chemotherapeutic agent than the standard of care dosage.

In one embodiment, a compound of Formula I, II, III, or IV, as described herein, is provided for use in treating a non-small cell lung carcinoma (NSCLC). In one embodiment, a method is provided to treat a host with non-small cell lung carcinoma (NSCLC) comprising administering to the host an effective amount of a compound of Formula I, II, III, or IV in combination with one or more additional chemotherapeutic agents. In one embodiment of the invention, a method is provided to treat a host with cancer comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with another tyrosine kinase inhibitor. In one embodiment, the tyrosine kinase inhibitor is a fibroblast growth factor receptor (FGFR) inhibitor. In one embodiment, the FGFR inhibitor is AZD-4547. In one embodiment, the cancer is non-small cell lung carcinoma (NSCLC). In some embodiments of the invention, a method is provided to treat a host with non-small cell lung carcinoma (NSCLC) comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with an additional tyrosine kinase inhibitor, wherein the Mer TKI is selected from the group consisting of UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A, and wherein the additional tyrosine kinase inhibitor is selected from the group consisting of gefitinib and crizotinib.

In one embodiment, a compound of Formula I, II, III, or IV, as described herein, is provided for use in treating a melanoma. In one embodiment, the administration of the Mer TKI compound described herein is combined with a chemotherapeutic agent. In one embodiment, the chemotherapeutic agent is an anti-programmed cell death-1 (PD-1) agent. In one embodiment, the chemotherapeutic agent is a B-RAF inhibitor. In one embodiment, the B-RAF inhibitor is vemurafenib. In one embodiment, the host does not have a melanoma with a B-RAF mutation. In one embodiment, the host has a melanoma with a B-RAF mutation. In one embodiment, the host has a melanoma with a RAS mutation. In one embodiment, the melanoma over-expresses MerTK. In one embodiment, the melanoma has metastasized. In one embodiment, the MerTK inhibitory compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, a compound of Formula I, II, III, or IV, as described herein, is provided for use in treating Acute Lymphoblastic Leukemia (ALL). In one embodiment, a method is provided to treat a host with ALL comprising administering to the host an effective amount of a compound of Formula I, II, III, or IV in combination with methotrexate. In one embodiment, the MerTK inhibitory compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, a compound of Formula I, II, III, or IV, as described herein, is provided for use in treating Acute Myeloid Leukemia (AML). In one embodiment, the AML contains a wild type FLT3 protein. In one embodiment, the replication of the AML cells are dependent on FLT3 expression. In one embodiment, the AML contains a FLT3-ITD mutation. In one embodiment, the AML contains a FLT3-TKD mutation. In one embodiment, the AML contains both a FLT3-ITD and FLT3-TKD mutation. In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is administered to a host suffering from AML, wherein the AML contains a mutation within the FLT3-TKD at amino acid F691 or D835. In one embodiment, the MerTK inhibitory compound administered is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, a tumor survival-signal inhibiting amount (for example 0.5 to 150 mg/dose) of Mer TKI including compounds of the present invention is administered to a host alone or in combination with a chemotherapeutic agent and/or anti-cancer targeted agent. In an alternative embodiment, a tumor survival-signal inhibiting amount (for example, at least 150 mg/dose, and in some embodiments, at least 200, 250, 300, 350, 400, 450, or 500 mg/dosage or more) of Mer TKI including active compounds of the present invention is administered to a host alone or in combination with a chemotherapeutic agent and/or anti-cancer targeted agent. In one embodiment, the Mer TKI and the chemotherapeutic agent act synergistically. In one embodiment, the use of a Mer TKI in combination with a chemotherapeutic agent provides for increased anti-tumor effects without an increase in the standard of care dosage of the chemotherapeutic agent.

In one embodiment, the use of a Mer TKI including compounds of the present invention in combination with a chemotherapeutic provides for equivalent or increased anti-tumor effects utilizing a lower dosage of a chemotherapeutic agent than the standard of care dosage.

In one aspect of the invention, the Mer TKI including compounds of the present invention can be administered to a host with a cancer prior to, during, or after administration with a chemotherapeutic agent or exposure to ionizing radiation. In one embodiment, a host is administered an effective amount of a chemotherapeutic agent or ionizing radiation and subsequently administered a Mer TKI.

In one embodiment, a method is provided to treat a host with cancer comprising administering to the host an effective amount of a compound of Formula I, II, III, or IV in combination with an immunomodulatory agent. In one embodiment, the immunomodulatory agent is selected from the group consisting of a CTLA-4 inhibitor, PD-1 or anti-PD-1 ligand, IFN-alpha, IFN-beta, and a vaccine, for example, a cancer vaccine. In one embodiment, a method is provided to treat a host with cancer comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with Keytruda® (pembrolizumab). In one embodiment, a method is provided to treat a host with cancer comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with Opdivo (nivolumab). In one embodiment, a method is provided to treat a host with cancer comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with Yervoy® (ipilimumab). In some embodiments, a method is provided to treat a host with cancer comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with an immunomodulatory agent selected from the group consisting of pembrolizumab and ipilimumab, wherein the Mer TKI is selected from the group consisting of UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A, wherein the cancer is melanoma.

In one embodiment, the Mer TKIs useful in the present invention, including active compounds of the present invention, are dual MER/FLT-3 TKIs. In one embodiment, the Mer TKIs are dual MER/Axl TKIs. In one embodiment, the Mer TKIs are MER-specific TKIs.

Tumors.

The active compounds and methods described herein are useful for the treatment of tumors. As contemplated herein, the cancer treated can be a primary tumor or a metastatic tumor. In one aspect, the methods described herein are used to treat a solid tumor, for example, melanoma, lung cancer (including lung adenocarcinoma, basal cell carcinoma, squamous cell carcinoma, large cell carcinoma, bronchioloalveolar carcinoma, bronchiogenic carcinoma, non-small-cell carcinoma, small cell carcinoma, mesothelioma); breast cancer (including ductal carcinoma, lobular carcinoma, inflammatory breast cancer, clear cell carcinoma, mucinous carcinoma, serosal cavities breast carcinoma); colorectal cancer (colon cancer, rectal cancer, colorectal adenocarcinoma); anal cancer; pancreatic cancer (including pancreatic adenocarcinoma, islet cell carcinoma, neuroendocrine tumors); prostate cancer; prostate adenocarcinoma; ovarian carcinoma (ovarian epithelial carcinoma or surface epithelial-stromal tumor including serous tumor, endometrioid tumor and mucinous cystadenocarcinoma, sex-cord-stromal tumor); liver and bile duct carcinoma (including hepatocellular carcinoma, cholangiocarcinoma, hemangioma); esophageal carcinoma (including esophageal adenocarcinoma and squamous cell carcinoma); oral and oropharyngeal squamous cell carcinoma; salivary gland adenoid cystic carcinoma; bladder cancer; bladder carcinoma; carcinoma of the uterus (including endometrial adenocarcinoma, ocular, uterine papillary serous carcinoma, uterine clear-cell carcinoma, uterine sarcomas and leiomyosarcomas, mixed mullerian tumors); glioma, glioblastoma, medullablastoma, and other tumors of the brain; kidney cancers (including renal cell carcinoma, clear cell carcinoma, Wilm's tumor); cancer of the head and neck (including squamous cell carcinomas); cancer of the stomach (gastric cancers, stomach adenocarcinoma, gastrointestinal stromal tumor); testicular cancer; germ cell tumor; neuroendocrine tumor; cervical cancer; carcinoids of the gastrointestinal tract, breast, and other organs; signet ring cell carcinoma; mesenchymal tumors including sarcomas, fibrosarcomas, haemangioma, angiomatosis, haemangiopericytoma, pseudoangiomatous stromal hyperplasia, myofibroblastoma, fibromatosis, inflammatory myofibroblastic tumor, lipoma, angiolipoma, granular cell tumor, neurofibroma, schwannoma, angio sarcoma, liposarcoma, rhabdomyosarcoma, osteosarcoma, leiomyoma, leiomysarcoma, skin, including melanoma, cervical, retinoblastoma, head and neck cancer, pancreatic, brain, thyroid, testicular, renal, bladder, soft tissue, adenal gland, urethra, cancers of the penis, myxosarcoma, chondrosarcoma, osteosarcoma, chordoma, malignant fibrous histiocytoma, lymphangiosarcoma, mesothelioma, squamous cell carcinoma; epidermoid carcinoma, malignant skin adnexal tumors, adenocarcinoma, hepatoma, hepatocellular carcinoma, renal cell carcinoma, hypernephroma, cholangiocarcinoma, transitional cell carcinoma, choriocarcinoma, seminoma, embryonal cell carcinoma, glioma anaplastic; glioblastoma multiforme, neuroblastoma, medulloblastoma, malignant meningioma, malignant schwannoma, neurofibrosarcoma, parathyroid carcinoma, medullary carcinoma of thyroid, bronchial carcinoid, pheochromocytoma, Islet cell carcinoma, malignant carcinoid, malignant paraganglioma, melanoma, Merkel cell neoplasm, cystosarcoma phylloide, salivary cancers, thymic carcinomas, and cancers of the vagina among others.

In some embodiments, a method is provided to treat a host with a glioblastoma comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with temozolomide, wherein the Mer TKI is selected from the group consisting of UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A. In some embodiments, a method is provided to treat a host with a breast cancer comprising administering to the host an effective amount of a Mer TKI including active compounds of the present invention in combination with trastuzumab, wherein the Mer TKI is selected from the group consisting of UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, the cancer is NSCLC. In one embodiment, the cancer is a melanoma. In one embodiment, the cancer is breast cancer. In one embodiment, the cancer is a glioblastoma. In one embodiment, the cancer is a bone cancer. In one embodiment, the cancer is a brain cancer. In one embodiment, the cancer is a colon cancer. In one embodiment, the cancer is a rectal cancer. In one embodiment, the cancer is an endometrial cancer. In one embodiment, the cancer is an esophageal cancer. In one embodiment, the cancer is a cancer of the gastrointestinal tract. In one embodiment, the cancer is a kidney cancer. In one embodiment, the cancer is a liver cancer. In one embodiment, the cancer is a lung cancer. In one embodiment, the cancer is a mantle cell lymphoma. In one embodiment, the cancer is an ovarian cancer. In one embodiment, the cancer is a pancreatic cancer. In one embodiment, the cancer is a pituitary cancer. In one embodiment, the cancer is a prostate cancer. In one embodiment, the cancer is a skeletal muscle cancer. In one embodiment, the cancer is a skin cancer. In one embodiment, the cancer is a stomach cancer. In one embodiment, the cancer is a thyroid cancer. In one embodiment, the cancer is a neuroendocrine cancer. In one embodiment, the cancer is a gastroesophageal cancer. In one embodiment, the cancer is a renal cell cancer. In one embodiment, the cancer is a head and neck cancer. In some embodiments, the Mer TKI used to treat a host having a cancer is selected from the group consisting of UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A.

In one embodiment, the methods described herein are useful for treating a host suffering from a lymphoma or lymphocytic or myelocytic proliferation disorder or abnormality. For example, the Mer TKIs as described herein can be administered to a subject suffering from a Hodgkin Lymphoma of a Non-Hodgkin Lymphoma. For example, the subject can be suffering from a Non-Hodgkin Lymphoma such as, but not limited to: an AIDS-Related Lymphoma; Anaplastic Large-Cell Lymphoma; Angioimmunoblastic Lymphoma; Blastic NK-Cell Lymphoma; Burkitt's Lymphoma; Burkitt-like Lymphoma (Small Non-Cleaved Cell Lymphoma); Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma; Cutaneous T-Cell Lymphoma; Diffuse Large B-Cell Lymphoma; Enteropathy-Type T-Cell Lymphoma; Follicular Lymphoma; Hepatosplenic Gamma-Delta T-Cell Lymphoma; Lymphoblastic Lymphoma; Mantle Cell Lymphoma; Marginal Zone Lymphoma; Nasal T-Cell Lymphoma; Pediatric Lymphoma; Peripheral T-Cell Lymphomas; Primary Central Nervous System Lymphoma; T-Cell Leukemias; Transformed Lymphomas; Treatment-Related T-Cell Lymphomas; or Waldenstrom's Macroglobulinemia.

Alternatively, the subject may be suffering from a Hodgkin Lymphoma, such as, but not limited to: Nodular Sclerosis Classical Hodgkin's Lymphoma (CHL); Mixed Cellularity CHL; Lymphocyte-depletion CHL; Lymphocyte-rich CHL; Lymphocyte Predominant Hodgkin Lymphoma; or Nodular Lymphocyte Predominant HL.

In one embodiment, the methods as described herein may be useful to treat a host suffering from a specific T-cell, a B-cell, or a NK-cell based lymphoma, proliferative disorder, or abnormality. For example, the subject can be suffering from a specific T-cell or NK-cell lymphoma, for example, but not limited to: Peripheral T-cell lymphoma, for example, peripheral T-cell lymphoma and peripheral T-cell lymphoma not otherwise specified (PTCL-NOS); anaplastic large cell lymphoma, for example anaplastic lymphoma kinase (ALK) positive, ALK negative anaplastic large cell lymphoma, or primary cutaneous anaplastic large cell lymphoma; angioimmunoblastic lymphoma; cutaneous T-cell lymphoma, for example mycosis fungoides, Sézary syndrome, primary cutaneous anaplastic large cell lymphoma, primary cutaneous CD30+ T-cell lymphoproliferative disorder; primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma; primary cutaneous gamma-delta T-cell lymphoma; primary cutaneous small/medium CD4+ T-cell lymphoma. and lymphomatoid papulosis; Adult T-cell Leukemia/Lymphoma (ATLL); Blastic NK-cell Lymphoma; Enteropathy-type T-cell lymphoma; Hematosplenic gamma-delta T-cell Lymphoma; Lymphoblastic Lymphoma; Nasal NK/T-cell Lymphomas; Treatment-related T-cell lymphomas; for example lymphomas that appear after solid organ or bone marrow transplantation; T-cell prolymphocytic leukemia; T-cell large granular lymphocytic leukemia; Chronic lymphoproliferative disorder of NK-cells; Aggressive NK cell leukemia; Systemic EBV+ T-cell lymphoproliferative disease of childhood (associated with chronic active EBV infection); Hydroa vacciniforme-like lymphoma; Adult T-cell leukemia/lymphoma; Enteropathy-associated T-cell lymphoma; Hepatosplenic T-cell lymphoma; or Subcutaneous panniculitis-like T-cell lymphoma.

Alternatively, the subject may be suffering from a specific B-cell lymphoma or proliferative disorder such as, but not limited to: multiple myeloma; Diffuse large B cell lymphoma; Follicular lymphoma; Mucosa-Associated Lymphatic Tissue lymphoma (MALT); Small cell lymphocytic lymphoma; Mantle cell lymphoma (MCL); Burkitt lymphoma; Mediastinal large B cell lymphoma; Waldenström macroglobulinemia; Nodal marginal zone B cell lymphoma (NMZL); Splenic marginal zone lymphoma (SMZL); Intravascular large B-cell lymphoma; Primary effusion lymphoma; or Lymphomatoid granulomatosis; Chronic lymphocytic leukemia/small lymphocytic lymphoma; B-cell prolymphocytic leukemia; Hairy cell leukemia; Splenic lymphoma/leukemia, unclassifiable; Splenic diffuse red pulp small B-cell lymphoma; Hairy cell leukemia-variant; Lymphoplasmacytic lymphoma; Heavy chain diseases, for example, Alpha heavy chain disease, Gamma heavy chain disease, Mu heavy chain disease; Plasma cell myeloma; Solitary plasmacytoma of bone; Extraosseous plasmacytoma; Primary cutaneous follicle center lymphoma; T cell/histiocyte rich large B-cell lymphoma; DLBCL associated with chronic inflammation; Epstein-Barr virus (EBV)+DLBCL of the elderly; Primary mediastinal (thymic) large B-cell lymphoma; Primary cutaneous DLBCL, leg type; ALK+ large B-cell lymphoma; Plasmablastic lymphoma; Large B-cell lymphoma arising in HHV8-associated multicentric; Castleman disease; B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma; B-cell lymphoma, unclassifiable, with features intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma; Nodular sclerosis classical Hodgkin lymphoma; Lymphocyte-rich classical Hodgkin lymphoma; Mixed cellularity classical Hodgkin lymphoma; or Lymphocyte-depleted classical Hodgkin lymphoma.

In one embodiment, the methods described herein can be used to a subject suffering from a leukemia. For example, the subject may be suffering from an acute or chronic leukemia of a lymphocytic or myelogenous origin, such as, but not limited to: Acute lymphoblastic leukemia (ALL); Acute myelogenous leukemia (AML); Chronic lymphocytic leukemia (CLL); Chronic myelogenous leukemia (CML); juvenile myelomonocytic leukemia (JMML); hairy cell leukemia (HCL); acute promyelocytic leukemia (a subtype of AML); T-cell prolymphocytic leukemia (TPLL); large granular lymphocytic leukemia; or Adult T-cell chronic leukemia; large granular lymphocytic leukemia (LGL). In one embodiment, the patient suffers from an acute myelogenous leukemia, for example an undifferentiated AML (M0); myeloblastic leukemia (M1; with/without minimal cell maturation); myeloblastic leukemia (M2; with cell maturation); promyelocytic leukemia (M3 or M3 variant [M3V]); myelomonocytic leukemia (M4 or M4 variant with eosinophilia [M4E]); monocytic leukemia (M5); crythroleukemia (M6); or megakaryoblastic leukemia (M7).

Acute Myeloid Leukemia.

In one embodiment, the methods described herein can be used to treat a host suffering from Acute Myeloid Leukemia (AML). In one embodiment, the AML contains a wild type FLT3 protein. In one embodiment, the replication of the AML cells are dependent on FLT3 expression. In one embodiment, the AML contains a FLT3-ITD mutation. In one embodiment, the AML contains a FLT3-TKD mutation. In one embodiment, the AML contains both a FLT3-ITD and FLT3-TKD mutation.

FLT3-ITD mutations are well known in the art. FLT3-TKD mutations are also well known in the art. In one embodiment, a FLT3 or dual MER/FLT3 inhibitor is administered to a host suffering from AML, wherein the AML contains a mutation within the FLT3-TKD at amino acid F691 or D835. In one embodiment, the FLT3-TKD mutation is selected from D835H, D835N, D835Y, D835A, D835V, D835V, D835E, I836F, I836L, I836V, I836D, I836H, I836M, and F691L. In one embodiment, the host is suffering from the FLT3-TKD mutation D835Y. In one embodiment, the host is suffering from the FLT3-TKD mutation F691L.

In one embodiment, the host is suffering from acute promyelocytic leukemia (a subtype of AML); a minimally differentiated AML (M0); myeloblastic leukemia (M1; with/without minimal cell maturation); myeloblastic leukemia (M2; with cell maturation); promyelocytic leukemia (M3 or M3 variant [M3V]); myelomonocytic leukemia (M4 or M4 variant with eosinophilia [M4E]); monocytic leukemia (M5); erythroleukemia (M6); or megakaryocytic leukemia (M7). In one embodiment, the host is suffering from AML that has relapsed or become refractory to previous treatments. In one embodiment, the host has previously been treated with a FLT3 inhibitor or other chemotherapeutic agent.

In one embodiment, the FLT3 inhibitors are efficacious against AML having both FLT3-ITD and FLT3-TKD mutations, wherein resistance to other FLT3 inhibitors, for example, AC220, has been established.

In one embodiment, the host has an Acute Myeloid Leukemia (AML) comprising a FLT3 mutation, wherein the mutation confers resistance to a FLT3 inhibitor other than the FLT3 inhibitors described herein. In one embodiment, the host has a AML comprising a FLT3 mutation, wherein the mutation has conferred resistance to quizartinib (AC220) or other FLT3 inhibitor selected from lestaurtinib, sunitinib, sorafenib, tandutinib, midostaurin, amuvatinib crenolanib, dovitinib, ENMD-2076 (Entremed), or KW-2449 (Kyowa Hakko Kirin), or a combination thereof.

Chemotherapeutic Agents.

In one embodiment, an active compound or Mer TKI as described herein is used in combination or alternation with a chemotherapeutic agent. Such agents may include, but are not limited to, tamoxifen, midazolam, letrozole, bortezomib, anastrozole, goserelin, an mTOR inhibitor, a PI3 kinase inhibitors, dual mTOR-PI3K inhibitors, MEK inhibitors, RAS inhibitors, ALK inhibitors, HSP inhibitors (for example, HSP70 and HSP 90 inhibitors, or a combination thereof). Examples of mTOR inhibitors include but are not limited to rapamycin and its analogs, everolimus (Afinitor), temsirolimus, ridaforolimus, sirolimus, and deforolimus. Examples of P13 kinase inhibitors include but are not limited to Wortmannin, demethoxyviridin, perifosine, idelalisib, PX-866, IPI-145, BAY 80-6946, BEZ235, RP6503, TGR 1202 (RP5264), MLN1117 (INK1117), Pictilisib, Buparlisib, SAR245408 (XL147), SAR245409 (XL765), Palomid 529, ZSTK474, PWT33597, RP6530, CUDC-907, and AEZS-136. Examples of MEK inhibitors include but are not limited to Tametinib, Selumetinib, MEK162, GDC-0973 (XL518), and PD0325901. Examples of RAS inhibitors include but are not limited to Reolysin and siG12D LODER. Examples of ALK inhibitors include but are not limited to Crizotinib, AP26113, and LDK378. HSP inhibitors include but are not limited to Geldanamycin or 17-N-Allylamino-17-demethoxygeldanamycin (17AAG), and Radicicol. In one embodiment, the chemotherapeutic agent is an anti-programmed cell death-1 (PD-1) agent, for example, nivolumab, pembrolizumab, BMS936559, lambrolizumab, MPDL3280A, pidilizumab, AMP-244, and MEDI4736. In one embodiment, the chemotherapeutic agent is a B-RAF inhibitor, for example, vemurafenib or sorafenib. In one embodiment, the chemotherapeutic agent is a FGFR inhibitor, for example, but not limited to, AZD4547, dovitinib, BGJ398, LY2874455, and ponatinib. In one embodiment, an active compound or Mer TKI as described herein is used in combination with crizotinib.

In certain aspects, the additional therapeutic agent is an anti-inflammatory agent, a chemotherapeutic agent, a radiotherapeutic, an additional therapeutic agent, or an immunosuppressive agent.

Suitable chemotherapeutic agents include, but are not limited to, radioactive molecules, toxins, also referred to as cytotoxins or cytotoxic agents, which includes any agent that is detrimental to the viability of cells, agents, and liposomes or other vesicles containing chemotherapeutic compounds. General anticancer pharmaceutical agents include: Vincristine (Oncovin®) or liposomal vincristine (Margibo®), Daunorubicin (daunomycin or Cerubidine®) or doxorubicin (Adriamycin®), Cytarabine (cytosine arabinoside, ara-C, or Cytosar®), L-asparaginase (Elspar®) or PEG-L-asparaginase (pegaspargase or Oncaspar®), Etoposide (VP-16), Teniposide (Vumon®), 6-mercaptopurine (6-MP or Purinethol®), Methotrexate, Cyclophosphamide (Cytoxan®), Prednisone, Dexamethasone (Decadron), imatinib (Gleevec®), dasatinib (Sprycel®), nilotinib (Tasigna®), bosutinib (Bosulif®), and ponatinib (Iclusig™). Examples of additional suitable chemotherapeutic agents include but are not limited to 1-dehydrotestosterone, 5-fluorouracil decarbazine, 6-mercaptopurine, 6-thioguanine, actinomycin D, adriamycin, aldesleukin, alkylating agents, allopurinol sodium, altretamine, amifostine, anastrozole, anthramycin (AMC)), anti-mitotic agents, cis-dichlorodiamine platinum (II) (DDP) cisplatin), diamino dichloro platinum, anthracyclines, antibiotics, antimetabolites, asparaginase, BCG live (intravesical), betamethasone sodium phosphate and betamethasone acetate, bicalutamide, bleomycin sulfate, busulfan, calcium leucouorin, calicheamicin, capecitabine, carboplatin, lomustine (CCNU), carmustine (BSNU), Chlorambucil, Cisplatin, Cladribine, Colchicin, conjugated estrogens, Cyclophosphamide, Cyclothosphamide, Cytarabine, Cytarabine, cytochalasin B, Cytoxan, Dacarbazine, Dactinomycin, dactinomycin (formerly actinomycin), daunirubicin HCL, daunorucbicin citrate, denileukin diftitox, Dexrazoxane, Dibromomannitol, dihydroxy anthracin dione, Docetaxel, dolasetron mesylate, doxorubicin HCL, dronabinol, E. coli L-asparaginase, emetine, epoetin-α, Erwinia L-asparaginase, esterified estrogens, estradiol, estramustine phosphate sodium, ethidium bromide, ethinyl estradiol, etidronate, etoposide citrororum factor, etoposide phosphate, filgrastim, floxuridine, fluconazole, fludarabine phosphate, fluorouracil, flutamide, folinic acid, gemcitabine HCL, glucocorticoids, goserelin acetate, gramicidin D, granisetron HCL, hydroxyurea, idarubicin HCL, ifosfamide, interferon α-2b, irinotecan HCL, letrozole, leucovorin calcium, leuprolide acetate, levamisole HCL, lidocaine, lomustine, maytansinoid, mechlorethamine HCL, medroxyprogesterone acetate, megestrol acetate, melphalan HCL, mercaptipurine, mesna, methotrexate, methyltestosterone, mithramycin, mitomycin C, mitotane, mitoxantrone, nilutamide, octreotide acetate, oligomycin A, ondansetron HCL, paclitaxel, pamidronate disodium, pentostatin, pilocarpine HCL, plimycin, polifeprosan 20 with carmustine implant, porfimer sodium, procaine, procarbazine HCL, propranolol, rituximab, sargramostim, streptozotocin, tamoxifen, taxol, teniposide, tenoposide, testolactone, tetracaine, thioepa chlorambucil, thioguanine, thiotepa, topotecan HCL, toremifene citrate, trastuzumab, tretinoin, valrubicin, vinblastine sulfate, vincristine sulfate, and vinorelbine tartrate. In one embodiment, an active compound or Mer TKI as described herein is used in combination with oligomycin A.

Additional therapeutic agents that can be administered in combination with a compound disclosed herein can include bevacizumab, sutinib, sorafenib, 2-methoxyestradiol or 2ME2, finasunate, vatalanib, vandetanib, aflibercept, volociximab, etaracizumab (MEDI-522), cilengitide, erlotinib, cetuximab, panitumumab, gefitinib, trastuzumab, dovitinib, figitumumab, atacicept, rituximab, alemtuzumab, aldesleukine, atlizumab, tocilizumab, temsirolimus, everolimus, lucatumumab, dacetuzumab, HLL1, huN901-DM1, atiprimod, natalizumab, bortezomib, carfilzomib, marizomib, tanespimycin, saquinavir mesylate, ritonavir, nelfinavir mesylate, indinavir sulfate, belinostat, panobinostat, mapatumumab, lexatumumab, dulanermin, ABT-737, oblimersen, plitidepsin, talmapimod, P276-00, enzastaurin, tipifarnib, perifosine, imatinib, dasatinib, lenalidomide, thalidomide, simvastatin, ABT-888, temozolomide, erlotinib, lapatinib, sunitinib, FTS, AZD6244, BEZ235, and celecoxib. In one embodiment, an active compound or Mer TKI as described herein is used in combination with gefitinib.

In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with a chemotherapeutic agent for the treatment of AML. Such agents may include, but are not limited to, cytarabine (ara-C), anthracycline drugs including but not limited to, daunorubicin, idarubicin; cladribine, fludarabine, Gleevec® (imatinib), Sprycel® (dasatinib), adriamycin, arsenic trioxide, cerubidine, clafen, cyclophosphamide, cytarabine, daunorubicin, doxorubicin, vincristine, and topotecan. Some of the other chemo drugs that may be used to treat AML include: etoposide (VP-16), 6-thioguanine (6-TG), hydroxyurea (Hydrea®), Corticosteroid drugs, such as prednisone or dexamethasone (Decadron®), methotrexate (MTX), 6-mercaptopurine (6-MP), azacitidine (Vidaza®), and decitabine (Dacogen®). In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with cytarabine.

In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with an additional FLT3 inhibitor to treat with a host suffering from AML. Additional FLT3 inhibitors for use in combination with the FLT3 or dual MER/FLT3 inhibitors described herein include lestaurtinib, sunitinib, sorafenib, tandutinib, midostaurin, crenolanib, dovitinib, ENMD-2076 (Entremed), amuvatinib, or KW-2449 (Kyowa Hakko Kirin).

In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with a Ras inhibitor. Examples of RAS inhibitors include but are not limited to Reolysin, FusOn-H2, and siG12D LODER.

In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with a Phosphoinositide 3-kinase inhibitor (PI3K inhibitor). PI3K inhibitors that may be used in the present invention are well known. Examples of PI3K inhibitors include but are not limited to Wortmannin, demethoxyviridin, perifosine, idelalisib, Pictilisib, Palomid 529, ZSTK474, PWT33597, CUDC-907, AEZS-136, PX-866, IPI-145, RP6503, SAR245408 (XL147), duvelisib, GS-9820, GDC-0032 (2-[4-[2-(2-Isopropyl-5-methyl-1,2,4-triazol-3-yl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepin-9-yl]pyrazol-1-yl]-2-methylpropanamide), MLN-1117 ((2R)-1-Phenoxy-2-butanyl hydrogen (S)-methylphosphonate; or Methyl(oxo) {[(2R)-1-phenoxy-2-butanyl]oxy}phosphonium)), BYL-719 ((2S)—N1-[4-Methyl-5-[2-(2,2,2-trifluoro-1,1-dimethylethyl)-4-pyridinyl]-2-thiazolyl]-1,2-pyrrolidinedicarboxamide), GSK2126458 (2,4-Difluoro-N-{2-(methyloxy)-5-[4-(4-pyridazinyl)-6-quinolinyl]-3-pyridinyl}benzenesulfonamide), TGX-221 ((±)-7-Methyl-2-(morpholin-4-yl)-9-(1-phenylaminoethyl)-pyrido[1,2-a]-pyrimidin-4-one), GSK2636771 (2-Methyl-1-(2-methyl-3-(trifluoromethyl)benzyl)-6-morpholino-1H-benzo[d]imidazole-4-carboxylic acid dihydrochloride), KIN-193 ((R)-2-(0-(7-methyl-2-morpholino-4-oxo-4H-pyrido[1,2-a]pyrimidin-9-yl)ethyl)amino)benzoic acid), TGR-1202/RP5264, GS-9820 ((S)-1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-mohydroxypropan-1-one), GS-1101 (5-fluoro-3-phenyl-2-([S)]-1-[9H-purin-6-ylamino]-propyl)-3H-quinazolin-4-one), AMG-319, GSK-2269557, SAR245409 (N-(4-(N-(3-((3,5-dimethoxyphenyl)amino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methoxy-4 methylbenzamide), BAY80-6946 (2-amino-N-(7-methoxy-8-(3-morpholinopropoxy)-2,3-dihydroimidazo[1,2-c]quinaz), AS 252424 (5-[1-[5-(4-Fluoro-2-hydroxy-phenyl)-furan-2-yl]-meth-(Z)-ylidene]-thiazolidine-2,4-dione), CZ 24832 (5-(2-amino-8-fluoro-[1,2,4]triazolo[1,5-a]pyridin-6-yl)-N-tert-butylpyridine-3-sulfonamide), Buparlisib (5-[2,6-Di(4-morpholinyl)-4-pyrimidinyl]-4-(trifluoromethyl)-2-pyridinamine), GDC-0941 (2-(1H-Indazol-4-yl)-6-[[4-(methylsulfonyl)-1-piperazinyl]methyl]-4-(4-morpholinyl)thieno[3,2-d]pyrimidine), GDC-0980 ((S)-1-(4-((2-(2-aminopyrimidin-5-yl)-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-6 yl)methyl)piperazin-1-yl)-2-hydroxypropan-1-one (also known as RG7422)), SF1126 ((8S,14S,17S)-14-(carboxymethyl)-8-(3-guanidinopropyl)-17-(hydroxymethyl)-3,6,9,12,15-pentaoxo-1-(4-(4-oxo-8-phenyl-4H-chromen-2-yl)morpholino-4-ium)-2-oxa-7,10,13,16-tetraazaoctadecan-18-oate), PF-05212384 (N-[4-[[4-(Dimethylamino)-1-piperidinyl]carbonyl]phenyl]-N′-[4-(4,6-di-4-morpholinyl-1,3,5-triazin-2-yl)phenyl]urea), LY3023414, BEZ235 (2-Methyl-2-{4-[3-methyl-2-oxo-8-(quinolin-3-yl)-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl]phenyl}propanenitrile), XL-765 (N-(3-(N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)sulfamoyl)phenyl)-3-methoxy-4-methylbenzamide), and GSK1059615 (5-[[4-(4-Pyridinyl)-6-quinolinyl]methylene]-2,4-thiazolidenedione), PX886 ([(3aR,6E,9S,9aR,10R,11aS)-6-[[bis(prop-2-enyl)amino]methylidene]-5-hydroxy-9-(methoxymethyl)-9a,11a-dimethyl-1,4,7-trioxo-2,3,3a,9,10,11-hexahydroindeno[4,5h]isochromen-10-yl]acetate (also known as sonolisib)), and the structure described in WO2014/071109 having the formula:

In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with a modulator of the STATS pathway. Compounds which modulate the Janus Kinase 2 (JAK2)—Signal Transducer and Activator of Transcription 5 (STATS) pathway include but are not limited to Lestaurtinib, Ruxolitinib, SB1518, CYT387, LY3009104, INC424, LY2784544, BMS-911543, NS-018, and TG101348.

In one embodiment, a FLT3 or dual MER/FLT3 inhibitor described herein is used in combination with an AKT inhibitor, including but not limited to, MK-2206, GSK690693, Perifosine, (KRX-0401), GDC-0068, Triciribine, AZD5363, Honokiol, PF-04691502, and Miltefosine.

Immunomodulatory Combination Agents.

Active compounds as described herein used in a dosage for direct effect on the diseased cell can be used in combination with one or more immunotherapy agents for additive or synergistic efficacy against solid tumors. In one embodiment, a tumor associated macrophage MerTK inhibiting amount of a Mer TKI is used in combination or alternation with the immunomodulatory agent. In another embodiment, a host tumor survival-signal inhibiting, antiviral or antibacterial amount of a Mer TKI is used in combination or alternation with the immunomodulatory agent.

Immunomodulators are small molecules or biologic agents that treat a disease by inducing, enhancing or suppressing the host's immune system. In the present application, one or more immunomodulators are selected that induce or enhance the host's immune system. Some immunomodulators boost the host's immune system and others help train the host's immune system to better attack tumor cells. Other immunomodulators target proteins that help cancer grow.

Three general categories of immunotherapies are antibodies, cancer vaccines, and non-specific immunotherapies. Antibodies are typically administered as monoclonals, although that is not required. “Naked monoclonal antibodies” work by attaching to antigens on tumor cells. Some antibodies can act as a marker for the body's immune system to destroy the tumor cells. Others block signaling agents for tumor cells. Antibodies can generally be used to bind to any signaling or metabolic agent that directly or indirectly facilitates tumor growth. Examples are alemtuzumab (Campath) which binds to CD52 antigen, and trastuzumab (Herceptin), which binds to the HER2 protein.

In another embodiment, an antibody can be used that is conjugated to another moiety that increases it delivery or efficacy. For example, the antibody can be connected to a cytotoxic drug or a radiolabel. Conjugated antibodies are sometimes referred to as “tagged, labeled or loaded”. Radiolabeled antibodies have small radioactive particles attached to them. Examples are Zevalin, which is an antibody against CD20 used to treat lymphoma. Chemolabeled antibodies are antibodies that have cytotoxic agents attached to them. Examples are Adcetris, which targets CD30, and Kadcyla, which targets HER². Ontak, while not an antibody, is similar in that it is interleukin-2 attached to a toxin from diphtheria.

Another category of immunotherapy that can be used in the present invention is a cancer vaccine. Most cancer vaccines are prepared from tumor cells, parts of tumor cells or pure antigens. The vaccine can be used with an adjuvant to help boost the immune response. An example is Provenge, which is the first cancer vaccine approved by the US FDA. The vaccine can for example be a dendritic cell vaccine or a vector-based vaccine

Nonspecific tumor immunotherapies and adjuvants include compounds that stimulate the immune system to do a better job at attacking the tumor cells. Such immunotherapies include cytokines, interleukins, interferons (α primarily but can be also β or γ). Specific agents include granulocyte-macrophage colony-stimulating factor (GM-CSF), IL-12, IL-7, IL-21, drugs that target CTLA-4 (such as Yervoy, which is Ipilimumab) and drugs that target PD-1 or PDL-1 (such as for example, nivolumab (BMS), pembrolizumab (Merck), pidilizumab (CureTech/Teva), AMP-244 (Amplimmune/GSK), BMS-936559 (BMS), and MEDI4736 (Roche/Genentech)).

Other drugs that boost the immune system are thalidomide, lenalidomide, pomalidomide, the Bacille Calmette-Gurin bacteria and Imiquimod. Additional therapeutic agents that can be used in combination with the MerTK inhibitor include bispecific antibodies, chimeric antigen receptor (CAR) T-cell therapy and tumor-infiltrating lymphocytes.

In one aspect of the present invention, a compound described herein can be combined with at least one immunosuppressive agent. The immunosuppressive agent is preferably selected from the group consisting of a calcineurin inhibitor, e.g. a cyclosporin or an ascomycin, e.g. Cyclosporin A (NEORAL®), FK506 (tacrolimus), pimecrolimus, a mTOR inhibitor, e.g. rapamycin or a derivative thereof, e.g. Sirolimus (RAPAMUNE®), Everolimus (Certican®), temsirolimus, zotarolimus, biolimus-7, biolimus-9, a rapalog, e.g.ridaforolimus, azathioprine, campath 1H, a SIP receptor modulator, e.g. fingolimod or an analogue thereof, an anti IL-8 antibody, mycophenolic acid or a salt thereof, e.g. sodium salt, or a prodrug thereof, e.g. Mycophenolate Mofetil (CELLCEPT®), OKT3 (ORTHOCLONE OKT3®), Prednisone, ATGAM®, THYMOGLOBULIN®, Brequinar Sodium, OKT4, T10B9.A-3A, 33B3.1, 15-deoxyspergualin, tresperimus, Leflunomide ARAVA®, CTLAI-Ig, anti-CD25, anti-IL2R, Basiliximab (SIMULECT®), Daclizumab (ZENAPAX®), mizorbine, methotrexate, dexamethasone, ISAtx-247, SDZ ASM 981 (pimecrolimus, Elidel®), CTLA41 g (Abatacept), belatacept, LFA31 g, etanercept (sold as Enbrel® by Immunex), adalimumab (Humira®), infliximab (Remicade®), an anti-LFA-1 antibody, natalizumab (Antegren®), Enlimomab, gavilimomab, antithymocyte immunoglobulin, siplizumab, Alefacept efalizumab, pentasa, mesalazine, asacol, codeine phosphate, benorylate, fenbufen, naprosyn, diclofenac, etodolac and indomethacin, aspirin and ibuprofen.

7. Anti-Platelet Agents

In another embodiment, a compound described herein is used in the treatment of blot clot (thrombus) formation in a host in need thereof. In one embodiment, the host is suffering from coronary artery disease, peripheral vascular disease, or cerebrovascular disease. In one embodiment, a compound described herein is administered to a host prior to any medical or surgical procedure in which diminished coagulation potential is desirable. In one embodiment, an active compound disclosed herein is administered in combination with another anti-thrombotic or anti-clotting agent.

In one embodiment, a compound of Formula I, II, III, or IV, or another compound, as described herein, is provided for use in treating blot clot (thrombus) formation in a subject in need thereof, comprising administering an active compound as described herein, or a pharmaceutically acceptable composition, salt, isotopic analog, or prodrug thereof. In one embodiment, the compound for use in treating blot clot (thrombus) formation in a subject in need thereof is selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A, including a pharmaceutically acceptable composition, salt, isotopic analog or prodrug thereof.

In one embodiment, the treatment of blood clot formation is in, for example, a subject with coronary artery disease, peripheral vascular disease, or cerebrovascular disease, or the treatment is given prior to any medical or surgical procedure in which diminished coagulation potential is desirable. Coronary artery disease includes, for example, any coronary dysfunction (pathological state) resulting from coronary artherosclerosis, i.e. partial or total occlusion of coronary vessels. The term also includes a range of various acute and chronical pathological states comprising stable and unstable angina pectoris (SAP and UAP, respectively), left ventricular dysfunction LVD, (congestive) heart failure CHF, myocardial death. Peripheral vascular disease includes, for example, occlusive or functional peripheral arterial disease (PAD). Examples of occlusive PAD include peripheral arterial occlusion, which may be acute, and Buerger's disease (thomboangiitis obliterans). Examples of functional PAD include Raynaud's disease, Raynaud's phenomenon, and acrocyanosis. Cerebrovascular disease includes, for example, any abnormality of the brain resulting from a pathologic process of a blood vessel. In one embodiment, the cerebrovascular disease is selected from cerebral ischemia, cerebral hemorrhage, ischemic stroke, hemorrhagic stroke, or ischemic reperfusion injury resulting from reintroduction of blood flow following cerebral ischemia or ischemic stroke. In one non-limiting embodiment, the medical or surgical procedure is pulmonary vein ablation.

In one embodiment, the treatment of blood clot formation is in a host having thrombi in blood vessels from pathologies or treatments including, for example, myocardial infarction, unstable angina, atrial fibrillation, stroke, renal damage, percutaneous translumenal coronary angioplasty, athreosclerosis, disseminated intravascular coagulation, sepsis, endotoxemia (i.e., the presence of endotoxins in the blood), pulmonary embolism and deep vein thrombosis. In one embodiment, the compounds described herein are administered to a host having blood clots on the surfaces of artificial organs, shunts and prostheses (for example, artificial heart valves that are implanted into a patient), and in patients that have received an intracoronary stent. In one embodiment, a host is administered an effective amount of a compound described herein due to the formation of clots resulting from some pathological conditions (for example, genetic mutation of VWF cleaving protease, ADAMT13), which may cause spontaneous binding of VWF to platelets resulting in formation of microthrombi in blood vessels leading to thrombotic thrombocytopenic purpura and other microangiopathy. Microangiopathy is a disease of blood vessels in which the walls of very small blood vessels (capillaries) become so thick and weak that they bleed, leak protein, and slow the flow of blood. In one embodiment, the treatment is in a patient with hemolytic uremic syndrome.

In one embodiment, an active compound disclosed herein is administered in combination with an additional anti-platelet agent. Examples of anti-platelet agents include, but are not limited to, aspirin, tirofiban (Aggrastat), Aggrenox, Agrylin, triflusal (Disgren), Flolan, eptifibatide (Integrilin), dipyridamole (Presantine), cilostazol (Pletal), abciximab (ReoPro), and Terutroban. In one embodiment, a compound selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A is administered in combination with an additional anti-platelet agent. In one embodiment, the Mer TKI and the additional anti-platelet agent act synergistically. In one embodiment, the use of a Mer TKI in combination with an additional anti-platelet agent provides for increased anti-thrombotic or anti-clotting effects without an increase in the standard of care dosage.

In one embodiment, the additional anti-platelet agent is an adenosine diphosphate (ADP) receptor inhibitor. Examples of ADP receptor inhibitors include, but are not limited to, clopidogrel (Plavix), prasugrel (Effient), ticagrelor (Brilinta), ticlopidine (Ticlid), N6-methyl-2′-deoxyadenosine-3′,5′-bisphosphate (MRS2179; P₂Y1 inhibitor), and 2-methylthioadenosine 5′-monophosphate triethylammonium salt (2-Me-SAMP; P₂Y12 inhibitor).

In one embodiment, an active compound disclosed herein is administered in combination with multiple anti-platelet agents. In one non-limiting embodiment, an active compound disclosed herein is administered in combination with N6-methyl-2′-deoxyadenosine-3′,5′-bisphosphate and 2-methylthioadenosine 5′-monophosphate triethylammonium salt.

In one embodiment, an active compound disclosed herein is administered in combination with an anti-coagulant. In one embodiment, the anti-coagulant is a heparin composition. In one embodiment, the heparin composition is a low molecular weight heparin composition. Low molecular weight heparin compositions are well known to those of skill in the art and include, but are not limited to, tinzaparin, certoparin, pamaparin, nadroparin, ardeparin, enoxaparin, reviparin, dalteparin, and fraxiparin. Additional examples of anti-coagulants include, but are not limited to, warfarin (Coumadin), Fragmin, Hep-Lock, Lovenox, and Miradon. In one embodiment, a compound selected from UNC3121A, UNC3194A, UNC2490A, UNC4171A, UNC4198A, UNC4337A, and UNC4340A is administered in combination with an anti-coagulant.

8. Nanoparticle Compositions or Carriers

In one aspect of the present invention, an effective amount of an active compound as described herein is incorporated into nanoparticles, e.g. for convenience of delivery and/or extended release delivery. The use of materials in nanoscale provides one the ability to modify fundamental physical properties such as solubility, diffusivity, blood circulation half-life, drug release characteristics, and immunogenicity. In the last two decades, a number of nanoparticle-based therapeutic and diagnostic agents have been developed for the treatment of cancer, diabetes, pain, asthma, allergy, and infections. These nanoscale agents can provide more effective and/or more convenient routes of administration, lower therapeutic toxicity, extend the product life cycle, and ultimately reduce health-care costs. As therapeutic delivery systems, nanoparticles allow targeted delivery and controlled release.

In addition, nanoparticle-based drug delivery can be used to release drugs at a sustained rate and thus lower the frequency of administration, deliver drugs in a target manner to minimize systemic side effects, or deliver two or more drugs simultaneously for combination therapy to generate a synergistic effect and suppress drug resistance. To date, a number of nanotechnology-based therapeutic products have been approved for clinical use. Among these products, liposomal drugs and polymer-based conjugates account for more than 80% of the products. See, Zhang, L., et al., Nanoparticles in Medicine: Therapeutic Applications and Developments, Clin. Pharm. and Ther., 83(5):761-769, 2008.

Optimal solid lipid nanoparticles (SLN) can be produced in a controlled fashion when a fraction of lipid in the crystalline alpha form can be created and preserved. By doing this, the SLN carrier has a built in trigger mechanism as lipids transform from the alpha to beta form and consequently control drug release. Drug release profiles can be modified according to the composition of the lipid matrix, surfactant concentration and production parameters. See, Muller, R. H., et al., Solid lipid nanoparticles (SLN) for controlled drug delivery—a review of the state of the art, Eur. H. Pharm. Biopharm., 50:161-177, 2000. Consien et al. have recently disclosed lipid nanoparticles having novel amino-lipids that form lipid nanoparticles and their use for the intracellular delivery of biologically active compounds, e.g., nucleic acids. See, U.S. Pat. No. 8,691,750 to Consien et al.

In regard to controlled release, Kanwar has recently disclosed alginate adsorbed chitosan adsorbed lactoferrin adsorbed calcium phosphate nanoparticles and the controlled release of lactoferrin from the nanoparticles. See, WO 2012/145801 to Kanwar. In addition, Armes et al. have recently disclosed polymer-templated core-shell nanoparticles adapted to facilitate controlled release of at least one active agent into a system in response to controlled changes in the pH of the system. See, U.S. Pat. No. 8,580,311 to Armes, S. et al. incorporated by reference herein.

Petros and DeSimone have recently reviewed strategies in the design of nanoparticles. In addition, the authors reviewed their PRINT (particle replication in non-wetting templates) technology for generating microparticles and nanoparticles. See, Petros, R. A. and DeSimone, J. M., Strategies in the design of nanoparticles for therapeutic applications, Nature Reviews/Drug Discovery, vol. 9:615-627, 2010. Importantly, the authors disclosed the production of nanoparticles in which a single parameter (shape or size) can be altered independently of all other particle attributes. The authors concluded their paper by outlining several particle characteristics that have emerged as being central to the function of engineered nanoparticles. These parameters include particle size, particle shape, surface characteristics and the ability to release therapeutics. Additional nanoparticle fabrication methods can also be found in U.S. Pat. No. 8,465,775, U.S. Pat. No. 8,444,899, U.S. Pat. No. 8,420,124, U.S. Pat. No. 8,263,129, U.S. Pat. Nos. 8,158,728 and 8,268,446 all hereby incorporated by reference.

Nanoparticles may be prepared using a wide variety of methods known in the art. For example, nanoparticles can be formed by methods as nanoprecipitation, flow focusing fluidic channels, spray drying, single and double emulsion solvent evaporation, solvent extraction, phase separation, milling, microemulsion procedures, microfabrication, nanofabrication, sacrificial layers, simple and complex coacervation, and other methods well known to those of ordinary skill in the art. Alternatively or additionally, aqueous and organic solvent syntheses for monodisperse semiconductor, conductive, magnetic, organic, and other nanomaterials have been described (Pellegrino et al., 2005, Small, 1:48; Murray et al., 2000, Ann. Rev. Mat. Sci., 30:545; and Trindade et al., 2001, Chem. Mat., 13:3843). Additional methods have been described in the literature (see, e.g., Doubrow, Ed., “Microcapsules and Nanoparticles in Medicine and Pharmacy,” CRC Press, Boca Raton, 1992; Mathiowitz et al., 1987, J. Control. Release, 5:13; Mathiowitz et al., 1987, Reactive Polymers, 6:275; and Mathiowitz et al., 1988, J. Appl. Polymer Sci., 35:755; U.S. Pat. Nos. 5,578,325 and 6,007,845; P. Paolicelli et al., “Surface-modified PLGA-based Nanoparticles that can Efficiently Associate and Deliver Virus-like Particles” Nanomedicine. 5(6):843-853 (2010)).

In some embodiments, the compounds described herein are associated with a nanoparticle, such as a polymeric nanoparticle. Nanoparticles may comprise natural polymers, including but not limited to chitosan, alginate, dextran, gelatin, and albumin, and synthetic polymers such as, but not limited to, poly(lactide-co-glycolide) (PLGA), (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), poly(sebacic anhydride), poly(ε-caprolactone), polystyrene, thermoresponsive (i.e., NIPAAm and CMCTS-g-PDEA) and pH-responsive (i.e., Eudragit L100, Eudragit S and AQOAT AS-MG) polymers.

In one embodiment, the polymeric particle is between about 0.1 nm to about 10000 nm, between about 1 nm to about 1000 nm, between about 10 nm and 1000 nm, between about 100 nm and 800 nm, between about 400 nm and 600 nm, or about 500 nm. In one embodiment, the micro-particles are about 0.1 nm, 0.5 nm, 1.0 nm, 5.0 nm, 10 nm, 25 urn, 50 nm, 75 nm, 100 nm, 150 nm, 200 nm, 250 nm, 300 nm, 400 nm, 450 nm, 500 nm, 550 nm, 600 nm, 650 nm, 700 nm, 750 nm, 800 nm, 850 nm, 900 nm, 950 nm, 1000 nm, 1250 nm, 1500 nm, 1750 nm, or 2000 nm. In one embodiment, the compounds described herein are covalently coupled to a polystyrene particle, PLGA particle, PLA particle, or other nanoparticle.

In some embodiments, the nanoparticle can be solid or hollow and can comprise one or more layers. In some embodiments, each layer has a unique composition and unique properties relative to the other layer(s). To give but one example, the nanoparticle may have a core/shell structure, wherein the core is one layer (e.g. a polymeric core) and the shell is a second layer (e.g. a lipid bilayer or monolayer). In some embodiments, the nanoparticle may comprise a plurality of different layers. In some embodiments, the compounds described herein can be incorporated into or surrounded by one or more layers.

In some embodiments, the nanoparticles comprising the compounds described herein may optionally comprise one or more lipids. In some embodiments, a nanoparticle may comprise a liposome. In some embodiments, a nanoparticle may comprise a lipid bilayer. In some embodiments, a nanoparticle may comprise a lipid monolayer. In some embodiments, a nanoparticle may comprise a micelle. In some embodiments, a nanoparticle may comprise a core comprising a polymeric matrix surrounded by a lipid layer (e.g., lipid bilayer, lipid monolayer, etc.). In some embodiments, a nanoparticle may comprise a non-polymeric core (e.g., metal particle, quantum dot, ceramic particle, bone particle, viral particle, proteins, nucleic acids, carbohydrates, etc.) surrounded by a lipid layer (e.g., lipid bilayer, lipid monolayer, etc.).

In other embodiments, the nanoparticle may comprise metal particles, quantum dots, ceramic particles, etc. In some embodiments, a non-polymeric nanoparticle is an aggregate of non-polymeric components, such as an aggregate of metal atoms (e.g., gold atoms).

In some embodiments, nanoparticles may optionally comprise one or more amphiphilic entities. In some embodiments, an amphiphilic entity can promote the production of nanoparticles with increased stability, improved uniformity, or increased viscosity. In some embodiments, amphiphilic entities can be associated with the interior surface of a lipid membrane (e.g., lipid bilayer, lipid monolayer, etc.). Many amphiphilic entities known in the art are suitable for use in making nanoparticles useful in the present invention. Such amphiphilic entities include, but are not limited to, phosphoglycerides; phosphatidylcholines; dipalmitoyl phosphatidylcholine (DPPC); dioleylphosphatidyl ethanolamine (DOPE); dioleyloxypropyltriethylammonium (DOTMA); dioleoylphosphatidylcholine; cholesterol; cholesterol ester; diacylglycerol; diacylglycerolsuccinate; diphosphatidyl glycerol (DPPG); hexanedecanol; fatty alcohols such as polyethylene glycol (PEG); polyoxyethylene-9-lauryl ether; a surface active fatty acid, such as palmitic acid or oleic acid; fatty acids; fatty acid monoglycerides; fatty acid diglycerides; fatty acid amides; sorbitan trioleate (Span® 85) glycocholate; sorbitan monolaurate (Span® 20); polysorbate 20 (Tween® 20); polysorbate 60 (Tween® 60); polysorbate 65 (Tween® 65); polysorbate 80 (Tween® 80); polysorbate 85 (Tween® 85); polyoxyethylene monostearate; surfactin; a poloxomer; a sorbitan fatty acid ester such as sorbitan trioleate; lecithin; lysolecithin; phosphatidylserine; phosphatidylinositol; sphingomyelin; phosphatidylethanolamine (cephalin); cardiolipin; phosphatidic acid; cerebrosides; dicetylphosphate; dipalmitoylphosphatidylglycerol; stearylamine; dodecylamine; hexadecyl-amine; acetyl palmitate; glycerol ricinoleate; hexadecyl sterate; isopropyl myristate; tyloxapol; poly(ethylene glycol)5000-phosphatidylethanolamine; poly(ethylene glycol)400-monostearate; phospholipids; synthetic and/or natural detergents having high surfactant properties; deoxycholates; cyclodextrins; chaotropic salts; ion pairing agents; and combinations thereof. An amphiphilic entity component may be a mixture of different amphiphilic entities. Those skilled in the art will recognize that this is an exemplary, not comprehensive, list of substances with surfactant activity. Any amphiphilic entity may be used in the production of nanoparticles to be used in accordance with the present invention.

In some embodiments, a nanoparticle may optionally comprise one or more carbohydrates. Carbohydrates may be natural or synthetic. A carbohydrate may be a derivatized natural carbohydrate. In certain embodiments, a carbohydrate comprises monosaccharide or disaccharide, including but not limited to glucose, fructose, galactose, ribose, lactose, sucrose, maltose, trehalose, cellbiose, mannose, xylose, arabinose, glucoronic acid, galactoronic acid, mannuronic acid, glucosamine, galatosamine, and neuramic acid. In certain embodiments, a carbohydrate is a polysaccharide, including but not limited to pullulan, cellulose, microcrystalline cellulose, hydroxypropyl methylcellulose (HPMC), hydroxycellulose (HC), methylcellulose (MC), dextran, cyclodextran, glycogen, hydroxyethylstarch, carageenan, glycon, amylose, chitosan, N,O-carboxylmethylchitosan, algin and alginic acid, starch, chitin, inulin, konjac, glucommannan, pustulan, heparin, hyaluronic acid, curdlan, and xanthan. In some embodiments, the nanoparticle does not comprise (or specifically exclude) carbohydrates, such as a polysaccharide. In certain embodiments, the carbohydrate may comprise a carbohydrate derivative such as a sugar alcohol, including but not limited to mannitol, sorbitol, xylitol, erythritol, maltitol, and lactitol.

In some embodiments, the associated nanoparticle can comprise one or more polymers. In some embodiments, the nanoparticle comprises one or more polymers that are a non-methoxy-terminated, pluronic polymer. In some embodiments, at least 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, or 99% (weight/weight) of the polymers that make up the nanoparticles are non-methoxy-terminated, pluronic polymers. In some embodiments, all of the polymers that make up the nanoparticle are non-methoxy-terminated, pluronic polymers. In some embodiments, the nanoparticle comprises one or more polymers that are a non-methoxy-terminated polymer. In some embodiments, at least 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, or 99% (weight/weight) of the polymers that make up the nanoparticles are non-methoxy-terminated polymers. In some embodiments, all of the polymers that make up the nanoparticle are non-methoxy-terminated polymers. In some embodiments, the nanoparticle comprises one or more polymers that do not comprise pluronic polymer. In some embodiments, at least 1%, 2%, 3%, 4%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, or 99% (weight/weight) of the polymers that make up the nanoparticle do not comprise pluronic polymer. In some embodiments, all of the polymers that make up the nanoparticles do not comprise pluronic polymer. In some embodiments, such a polymer can be surrounded by a coating layer (e.g., liposome, lipid monolayer, micelle, etc.). In some embodiments, various elements of the nanoparticle can be coupled with the polymer.

Other examples of polymers include, but are not limited to polyethylenes, polycarbonates (e.g. poly(1,3-dioxan-2one)), polyanhydrides (e.g. poly(sebacic anhydride)), polypropylfumerates, polyamides (e.g. polycaprolactam), polyacetals, polyethers, polyesters (e.g., polylactide, polyglycolide, polylactide-co-glycolide, polycaprolactone, polyhydroxyacid (e.g. poly((β-hydroxyalkanoate))), poly(orthoesters), polycyanoacrylates, polyvinyl alcohols, polyurethanes, polyphosphazenes, polyacrylates, polymethacrylates, polyureas, polystyrenes, and polyamines, polylysine, polylysine-PEG copolymers, and poly(ethyleneimine), poly(ethylene imine)-PEG copolymers.

In some embodiments, nanoparticles include polymers which have been approved for use in humans by the U.S. Food and Drug Administration (FDA) under 21 C.F.R. §177.2600, including but not limited to polyesters (e.g., polylactic acid, polylactic-co-glycolic acid), polycaprolactone, polyvalerolactone, poly(1,3-dioxan-2one)); polyanhydrides (e.g., poly(sebacic anhydride)); polyethers (e.g., polyethylene glycol); polyurethanes; polymethacrylates; polyacrylates; and polycyanoacrylates.

In some embodiments, polymers can be hydrophilic. For example, polymers may comprise anionic groups (e.g., phosphate group, sulphate group, carboxylate group); cationic groups (e.g., quaternary amine group); or polar groups (e.g., hydroxyl group, thiol group, amine group). In some embodiments, a nanoparticles comprising a hydrophilic polymeric matrix generates a hydrophilic environment within the nanoparticle. In some embodiments, polymers can be hydrophobic. In some embodiments, a nanoparticles comprising a hydrophobic polymeric matrix generates a hydrophobic environment within the nanoparticle. Selection of the hydrophilicity or hydrophobicity of the polymer may have an impact on the nature of materials that are incorporated (e.g., coupled) within the nanoparticle.

In some embodiments, polymers may be modified with one or more moieties and/or functional groups. A variety of moieties or functional groups can be used in accordance with the present invention. In some embodiments, polymers may be modified with polyethylene glycol (PEG), with a carbohydrate, and/or with acyclic polyacetals derived from polysaccharides (Papisov, 2001, ACS Symposium Series, 786:301). Certain embodiments may be made using the general teachings of U.S. Pat. No. 5,543,158 to Gref et al., or WO publication WO2009/051837 by Von Andrian et al.

In some embodiments, polymers may be modified with a lipid or fatty acid group. In some embodiments, a fatty acid group may be one or more of butyric, caproic, caprylic, capric, lauric, myristic, palmitic, stearic, arachidic, behenic, or lignoceric acid. In some embodiments, a fatty acid group may be one or more of palmitoleic, oleic, vaccenic, linoleic, alpha-linoleic, gamma-linoleic, arachidonic, gadoleic, arachidonic, eicosapentaenoic, docosahexaenoic, or erucic acid.

In some embodiments, polymers may be one or more acrylic polymers. In certain embodiments, acrylic polymers include, for example, acrylic acid and methacrylic acid copolymers, methyl methacrylate copolymers, ethoxyethyl methacrylates, cyanoethyl methacrylate, aminoalkyl methacrylate copolymer, poly(acrylic acid), poly(methacrylic acid), methacrylic acid alkylamide copolymer, poly(methyl methacrylate), poly(methacrylic acid anhydride), methyl methacrylate, polymethacrylate, poly(methyl methacrylate) copolymer, polyacrylamide, aminoalkyl methacrylate copolymer, glycidyl methacrylate copolymers, polycyanoacrylates, and combinations comprising one or more of the foregoing polymers. The acrylic polymer may comprise fully-polymerized copolymers of acrylic and methacrylic acid esters with a low content of quaternary ammonium groups.

In some embodiments, polymers can be cationic polymers. In general, cationic polymers are able to condense and/or protect negatively charged strands of nucleic acids (e.g. DNA, or derivatives thereof). Amine-containing polymers such as poly(lysine) (Zauner et al., 1998, Adv. Drug Del. Rev., 30:97; and Kabanov et al., 1995, Bioconjugate Chem., 6:7), poly(ethylene imine) (PEI; Boussif et al., 1995, Proc. Natl. Acad. Sci., USA, 1995, 92:7297), and poly(amidoamine) dendrimers (Kukowska-Latallo et al., 1996, Proc. Natl. Acad. Sci., USA, 93:4897; Tang et al., 1996, Bioconjugate Chem., 7:703; and Haensler et al., 1993, Bioconjugate Chem., 4:372) are positively-charged at physiological pH, form ion pairs with nucleic acids, and mediate transfection in a variety of cell lines. In embodiments, the nanoparticles may not comprise (or may exclude) cationic polymers.

In some embodiments, polymers can be degradable polyesters bearing cationic side chains (Putnam et al., 1999, Macromolecules, 32:3658; Barrera et al., 1993, J. Am. Chem. Soc., 115:11010; Kwon et al., 1989, Macromolecules, 22:3250; Lim et al., 1999, J. Am. Chem. Soc., 121:5633; and Zhou et al., 1990, Macromolecules, 23:3399). Examples of these polyesters include poly(L-lactide-co-L-lysine) (Barrera et al., 1993, J. Am. Chem. Soc., 115:11010), poly(serine ester) (Zhou et al., 1990, Macromolecules, 23:3399), poly(4-hydroxy-L-proline ester) (Putnam et al., 1999, Macromolecules, 32:3658; and Lim et al., 1999, J. Am. Chem. Soc., 121:5633), and poly(4-hydroxy-L-proline ester) (Putnam et al., 1999, Macromolecules, 32:3658; and Lim et al., 1999, J. Am. Chem. Soc., 121:5633).

The properties of these and other polymers and methods for preparing them are well known in the art (see, for example, U.S. Pat. Nos. 6,123,727; 5,804,178; 5,770,417; 5,736,372; 5,716,404; 6,095,148; 5,837,752; 5,902,599; 5,696,175; 5,514,378; 5,512,600; 5,399,665; 5,019,379; 5,010,167; 4,806,621; 4,638,045; and 4,946,929; Wang et al., 2001, J. Am. Chem. Soc., 123:9480; Lim et al., 2001, J. Am. Chem. Soc., 123:2460; Langer, 2000, Acc. Chem. Res., 33:94; Langer, 1999, J. Control. Release, 62:7; and Uhrich et al., 1999, Chem. Rev., 99:3181). More generally, a variety of methods for synthesizing certain suitable polymers are described in Concise Encyclopedia of Polymer Science and Polymeric Amines and Ammonium Salts, Ed. by Goethals, Pergamon Press, 1980; Principles of Polymerization by Odian, John Wiley & Sons, Fourth Edition, 2004; Contemporary Polymer Chemistry by Allcock et al., Prentice-Hall, 1981; Deming et al., 1997, Nature, 390:386; and in U.S. Pat. Nos. 6,506,577, 6,632,922, 6,686,446, and 6,818,732.

Polymers can be linear or branched polymers. In some embodiments, polymers can be dendrimers. In some embodiments, polymers can be substantially cross-linked to one another. In some embodiments, polymers can be substantially free of cross-links. In some embodiments, polymers can be used without undergoing a cross-linking step. It is further to be understood that a nanoparticle may comprise block copolymers, graft copolymers, blends, mixtures, and/or adducts of any of the foregoing and other polymers. Those skilled in the art will recognize that the polymers listed herein represent an exemplary, not comprehensive, list of polymers that can be of use in accordance with the present invention.

The compounds of the present invention can be coupled to a nanoparticle by any of a number of methods. Generally, the coupling can be a result of bonding between the compound and the nanoparticle. This bonding can result in the compound being attached to the surface of the nanoparticle and/or contained within (encapsulated) the nanoparticle. In some embodiments, however, the compounds are encapsulated by the nanoparticle as a result of the structure of the nanoparticle rather than bonding to the nanoparticle. In some embodiments, the nanoparticle comprises a polymer as provided herein, and the compounds described herein are coupled to the nanoparticle. The compounds described herein may be encapsulated into nanoparticles as desirable using a variety of methods including but not limited to C. Astete et al., “Synthesis and characterization of PLGA nanoparticles” J. Biomater. Sci. Polymer Edn, Vol. 17, No. 3, pp. 247-289 (2006); K. Avgoustakis “Pegylated Poly(Lactide) and Poly(Lactide-Co-Glycolide) Nanoparticles: Preparation, Properties and Possible Applications in Drug Delivery” Current Drug Delivery 1:321-333 (2004); C. Reis et al., “Nanoencapsulation I. Methods for preparation of drug-loaded polymeric nanoparticles” Nanomedicine 2:8-21 (2006); P. Paolicelli et al., “Surface-modified PLGA-based Nanoparticles that can Efficiently Associate and Deliver Virus-like Particles” Nanomedicine. 5(6):843-853 (2010). Other methods suitable for encapsulating the compounds described herein may be used, including without limitation methods disclosed in U.S. Pat. No. 6,632,671 to Unger Oct. 14, 2003.

In certain embodiments, nanoparticles are prepared by a nanoprecipitation process or spray drying. Conditions used in preparing nanoparticles may be altered to yield particles of a desired size or property (e.g., hydrophobicity, hydrophilicity, external morphology, “stickiness,” shape, etc.). The method of preparing the nanoparticles and the conditions (e.g., solvent, temperature, concentration, air flow rate, etc.) used may depend on the materials to be coupled to the nanoparticles and/or the composition of the polymer matrix. If particles prepared by any of the above methods have a size range outside of the desired range, particles can be sized, for example, using a sieve.

In one embodiment of the present invention, PRINT technology is used to manufacture nanoparticles comprising a compound described herein.

In another embodiment, provided herein are liposome based nanoparticles comprising a compound described herein. In another embodiment, a liposome based nanoparticle comprises a compound described herein formulated for controlled-release.

In one embodiment, provided herein are polymer based nanoparticles comprising a compound described herein. In another embodiment, provided herein are polymer based nanoparticles comprising a compound described herein formulated for controlled-release.

In one embodiment, nanoparticles are comprised of albumin and a compound described herein. In another embodiment, nanoparticles are comprised of a polysaccharide and a compound described herein. In one embodiment, nanoparticles are comprised of a metal and a compound described herein. In another embodiment, nanoparticles are comprised of gold and a compound described herein. In another embodiment, nanoparticles are comprised of iron oxide and a compound described herein. In one embodiment, nanoparticles are comprised of silicon and a compound described herein.

In regard to polymers used for the production of nanoparticles, several reviews are available. See, for example, Soppimath, K. S., et al., Biodegradable polymeric nanoparticles as drug delivery devices, J. Controlled Release, 70:1-20, 2001, Agnihotri, S. A., et al., Recent advances on chitosan-based micro- and nanoparticle delivery, J. Controlled Release, 100(1):5-28, 2004, Ganta, S, et al., A review of stimuli-responsive nanocarriers for drug and gene delivery, J. Controlled Release, 126(3):187-204, 2008, Danhier, F. et al., PLGA-based nanoparticles: An overview of biomedical applications, J. Controlled Release, 161(2):505-522, 2012,

In one embodiment, nanoparticles are comprised of L-glutamic acid copolymers and a compound described herein. In another embodiment, nanoparticles are comprised of L-alanine copolymers and a compound described herein. In one embodiment, nanoparticles are comprised of L-lysine copolymers and a compound described herein. In another embodiment, nanoparticles are comprised of L-tyrosine copolymers and a compound described herein. In other embodiment, nanoparticles are comprised of poly(lactic-co-glycolic acid) and a compound described herein. In another embodiment, nanoparticles are comprised of methoxy-PEG-poly(D,L-lactide) and a compound described herein. In another embodiment, nanoparticles are comprised of HPMA copolymer and a compound described herein. In one embodiment, nanoparticles are comprised of polycyclodextran and a compound described herein. In one embodiment, nanoparticles are comprised of polyglutamate and a compound described herein. In another embodiment, nanoparticles are comprised of poly(iso-hexyl-cyanoacrylate) and a compound described herein. In one embodiment, nanoparticles are comprised of poly-L-lysine and a compound described herein. In another embodiment, nanoparticles are comprised of PEG and a compound described herein. In one embodiment, nanoparticles are made of combinations of polymers and a compound described herein.

In one embodiment, a compounds described herein is released from a nanoparticle over a period of between about 1 and about 90 days. In one embodiment, the compound is released over a period of about 3 to 28 days. In one embodiment, the compound is released over a period of about 5 to 21 days.

EXAMPLES

The present invention is explained in greater detail in the following non-limiting Examples.

Example 1 Syntheses of Active Compounds General Schemes

Scheme 1 illustrates a general procedure for preparing a compound of the present invention. Structure 1-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 1-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 1-2 can be prepared by treating Structure 1-1 with a desired amine, R³—NH₂, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 150° C. under microwave irradiation for about 30 minutes. Structure 1-2 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 1-3 can be prepared by treating Structure 1-2 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in a mixture of organic solvents at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the mixture of organic solvents comprises water and N,N-dimethylformamide. Structure 1-4 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 1-4 can be prepared by treating Structure 1-3 with a desired acid. In one embodiment, the acid is 4N hydrochloric acid. Compounds of Formula II can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula II can be prepared by treating Structure 1-4 with a desired amine, for example, N-methylpiperazine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. This chemistry is illustrated in Scheme 1.

Scheme 2 illustrates a general procedure for preparing a compound of the present invention. Structure 2-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 2-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 2-2 can be prepared by treating Structure 2-1 with a desired amine R³—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 150° C. under microwave irradiation for about 30 minutes. Structure 2-2 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 2-3 can be prepared by treating Structure 2-2 with 5-(1,3-dioxolan)-2-pyridinyl trihydroxyborate lithium, copper bromide, a base, and an organometallic reagent in a mixture of organic solvents at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the mixture of organic solvents comprises water and N,N-dimethylformamide. Structure 2-4 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 2-4 can be prepared by treating Structure 2-3 with a desired acid. In one embodiment, the acid is 4N hydrochloric acid. Compounds of Formula II can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula II can be prepared by treating Structure 2-4 with a desired amine, for example, N-methylpiperazine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. This chemistry is illustrated in Scheme 2.

Scheme 3 illustrates a general procedure for preparing a compound of the present invention. Structure 3-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 3-1 can be prepared by treating a mixture of a commercially available 4-chloro-5-bromo-2-(methylthio)pyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 3-1 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 3-2 can be prepared by treating Structure 3-1 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in a mixture of organic solvents at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the mixture of organic solvents comprises water and N,N-dimethylformamide. Structure 3-3 can be prepared by oxidation of a desired thiol with a desired oxidizing agent according to methods known in the art. For example, Structure 3-3 can be prepared by treating Structure 3-2 with an oxidizing reagent, for example, m-chloroperbenzoic acid, in an organic solvent. In one embodiment, the organic solvent is tetrahydrofuran. Compounds of Formula II can be prepared by treating Structure 3-3 with a desired amine, R³—NH₂, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 150° C. under microwave irradiation for about 30 minutes. This chemistry is illustrated in Scheme 3.

Scheme 4 illustrates a general procedure for preparing a compound of the present invention. Structure 4-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 4-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 4-2 can be prepared by treating Structure 4-1 with a desired amine, R⁹R¹³NH, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 150° C. under microwave irradiation for about 30 minutes. Structure 4-2 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 4-3 can be prepared by treating Structure 4-2 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in a mixture of organic solvents at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the mixture of organic solvents comprises water and N,N-dimethylformamide. Structure 4-4 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 4-4 can be prepared by treating Structure 4-3 with a desired acid. In one embodiment, the acid is 4N hydrochloric acid. Compounds of Formula IV can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula IV can be prepared by treating Structure 4-4 with a desired amine, for example, N-methylpiperazine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. This chemistry is illustrated in Scheme 4.

Scheme 5 illustrates a general procedure for preparing a compound of the present invention. Structure 5-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 5-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 5-2 can be prepared by treating Structure 5-1 with a desired amine R⁹R¹³NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 150° C. under microwave irradiation for about 30 minutes. Structure 5-2 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 5-3 can be prepared by treating Structure 5-2 with 5-(1,3-dioxolan)-2-pyridinyl trihydroxyborate lithium, copper bromide, a base, and an organometallic reagent in a mixture of organic solvents at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]-dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the mixture of organic solvents comprises water and N,N-dimethylformamide. Structure 5-4 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 5-4 can be prepared by treating Structure 5-3 with a desired acid. In one embodiment, the acid is 4N hydrochloric acid. Compounds of Formula IV can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula IV can be prepared by treating Structure 5-4 with a desired amine, for example, N-methylpiperazine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. This chemistry is illustrated in Scheme 5.

Scheme 6 illustrates a general procedure for preparing a compound of the present invention. Structure 6-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 6-1 can be prepared by treating a mixture of a commercially available 4-chloro-5-bromo-2-(methylthio)pyrimidine and a desired amine R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 6-1 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 6-2 can be prepared by treating Structure 6-1 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in a mixture of organic solvents at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the mixture of organic solvents comprises water and N,N-dimethylformamide. Structure 6-3 can be prepared by oxidation of a desired thiol with a desired oxidizing agent according to methods known in the art. For example, Structure 6-3 can be prepared by treating Structure 6-2 with an oxidizing reagent, for example, m-chloroperbenzoic acid, in an organic solvent. In one embodiment, the organic solvent is tetrahydrofuran. Compounds of Formula IV can be prepared by treating Structure 6-3 with a desired amine, R⁹R¹³NH, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 150° C. under microwave irradiation for about 30 minutes. This chemistry is illustrated in Scheme 6.

Scheme 7 illustrates a general procedure for preparing a compound of the present invention. Structure 7-1 can be prepared by amination of a desired 5-substituted carbonyl chloride pyrimidine with a desired amine according to methods known in the art. For example, Structure 7-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired amine R¹—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, tetrahydrofuran, at about 0° C. Structure 7-2 can be prepared by treating Structure 7-1 with a desired amine, R²—NH₂, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. for about 90 minutes. Compounds of Formula I can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example compounds of Formula I can be prepared by treating Structure 7-2 with a desired amine, for example, R³—NH₂, a base and an organic solvent at about room temperature. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. This chemistry is illustrated in Scheme 7.

Scheme 8 illustrates a general procedure for preparing a compound of the present invention. Structure 8-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 8-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about room temperature. Structure 8-2 can be prepared by treating Structure 8-1 with a desired amine, R²—NH₂, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. for about 90 minutes. Structure 8-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example compounds of Structure 8-3 can be prepared by treating Structure 8-2 with a desired amine, for example, R³—NH₂, a base and an organic solvent at about room temperature. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. Structure 8-4 can be prepared by hydrolysis of a desired ester with a desired base according to methods known in the art. For example, Structure 8-3 can be treated with a base, for example lithium hydroxide in a mixture of solvents. In one embodiment, the mixture of solvents comprises water and methanol. Compounds of Formula I can be prepared by treating Structure 8-4 with an amine, a coupling reagent, a base and an organic solvent. In one embodiment, the amine is R¹—NH₂. In one embodiment, the coupling reagent is O-(benzotriazol-1-yl)-N,N,N′N′-tetramethyluronium tetrafluoroborate (TBTU). In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is N,N-dimethylformamide (DMF). This chemistry is illustrated in Scheme 8.

Scheme 9 illustrates a general procedure for preparing a compound of the present invention. Structure 9-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired amine according to methods known in the art. For example, Structure 9-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired amine R¹¹R¹⁴NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, tetrahydrofuran, at about 0° C. Structure 9-2 can be prepared by treating Structure 9-1 with a desired amine, R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. for about 90 minutes. Compounds of Formula III can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example compounds of Formula I can be prepared by treating Structure 9-2 with a desired amine, for example, R⁹R¹³NH, a base and an organic solvent at about room temperature. In one embodiment, the base is diisopropyl-ethylamine. In one embodiment, the organic solvent is 2-propanol. This chemistry is illustrated in Scheme 9.

Scheme 10 illustrates a general procedure for preparing a compound of the present invention. Structure 10-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 10-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about room temperature. Structure 10-2 can be prepared by treating Structure 10-1 with a desired amine, R¹⁰R¹²NH, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. for about 90 minutes. Structure 10-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example compounds of Structure 10-3 can be prepared by treating Structure 10-2 with a desired amine, for example, R⁹R¹³NH, a base and an organic solvent at about room temperature. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. Structure 10-4 can be prepared by hydrolysis of a desired ester with a desired base according to methods known in the art. For example, Structure 10-3 can be treated with a base, for example, lithium hydroxide, in a mixture of solvents. In one embodiment, the mixture of solvents comprises water and methanol. Compounds of Formula III can be prepared by treating Structure 10-4 with an amine, a coupling reagent, a base and an organic solvent. In one embodiment, the amine is R¹¹R¹⁴NH. In one embodiment, the coupling reagent is O-(benzotriazol-1-yl)-N,N,N′N′-tetramethyluronium tetrafluoroborate (TBTU). In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is N,N-dimethylformamide (DMF). This chemistry is illustrated in Scheme 10.

Scheme 11 illustrates a general procedure for preparing a compound of the present invention. Structure 11-1 can be prepared by amination of a desired 5-substituted carbonyl chloride pyrimidine with a desired amine according to methods known in the art. For example, Structure 11-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired amine R¹—NH₂ in the presence of two bases such as, for example, diisopropylethylamine and 4-dimethylaminopyridine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about 25° C. Structure 11-2 can be prepared by treating Structure 11-1 with a desired amine, R²—NH₂, in the presence of a base such as, for example, diisopropylethylamine, in a mixture of organic solvents such as, for example, 2-propanol and N,N-dimethylformamide (DMF), at about 25° C. for about 18 hours. The R² group can comprise an amino acid moiety that can have a protected amine that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Compounds of Formula I can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example compounds of Formula I can be prepared by treating Structure 11-2 with a desired amine, for example, R³—NH₂, a base and a mixture of organic solvents at about 45° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the mixture of organic solvents comprises 2-propanol and DMF. A compound of Formula I can be cyclized by amide bond formation by treating an amine with an acid according to methods known in the art. For example, a compound of Formula I can be treated with a coupling reagent, for example, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate, a base, for example, triethylamine, and a mixture of organic solvents, for example DMF and dichloromethane. The compound of Formula I can be treated with an organic acid such as trifluoroacetic acid and an organic solvent such as dichloromethane to remove a protecting group such as, for example, a Boc protecting group. This chemistry is illustrated in Scheme 11.

Scheme 12 illustrates a general procedure for preparing a compound of the present invention. Structure 12-1 can be prepared by amination of a desired 5-substituted carbonyl chloride pyrimidine with a desired amine according to methods known in the art. For example, Structure 12-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired amine R¹¹R¹⁴NH the presence of two bases such as, for example, diisopropylethylamine and 4-dimethylaminopyridine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about 25° C. Structure 12-2 can be prepared by treating Structure 12-1 with a desired amine, R¹⁰R¹²NH, in the presence of a base such as, for example, diisopropylethylamine, in a mixture of organic solvents such as, for example, 2-propanol and N,N-dimethylformamide (DMF), at about 25° C. for about 18 hours. The R¹² group can comprise an amino acid moiety that can have a protected amine that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Compounds of Formula III can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example compounds of Formula III can be prepared by treating Structure 12-2 with a desired amine, for example, R⁹R¹³NH, a base and a mixture of organic solvents at about 45° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the mixture of organic solvents comprises 2-propanol and DMF. A compound of Formula III can be cyclized by amide bond formation by treating an amine with an acid according to methods known in the art. For example, a compound of Formula III can be treated with a coupling reagent, for example, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate, a base, for example, triethylamine, and a mixture of organic solvents, for example DMF and dichloromethane. The compound of Formula III can be treated with an organic acid such as trifluoroacetic acid and an organic solvent such as dichloromethane to remove a protecting group such as, for example, a Boc protecting group. This chemistry is illustrated in Scheme 12.

Scheme 13 illustrates a general procedure for preparing a compound of the present invention. Structure 13-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 13-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about room temperature. Structure 13-2 can be prepared by treating Structure 13-1 with a desired amine, R²—NH₂, in the presence of a base such as, for example, diisopropylethylamine, and a mixture of organic solvents such as, for example, 2-propanol and dichloromethane at about 0° C. to about 25° C. for about 18 hours. The R² group can comprise an amino acid moiety that can comprise a protected amine that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. A compound of Structure 13-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 13-3 can be prepared by treating Structure 13-2 with a desired amine, for example, R³—NH₂, a base and a mixture of organic solvents at about 45° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the mixture of organic solvents comprises 2-propanol and DMF. Structure 13-3 can be cyclized by amide bond formation by treating an amine with an acid according to methods known in the art. For example, a compound of Structure 13-3 can be treated with a coupling reagent, for example, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU), a base, for example, triethylamine, and a mixture of organic solvents, for example DMF and dichloromethane. Structure 13-5 can be prepared by treatment of a desired ester with a desired base according to methods known in the art. For example, Structure 13-5 can be prepared by treating Structure 13-4 with a base such as lithium hydroxide and a mixture of solvents comprising water and tetrahydrofuran. A compound of Formula I can be prepared by forming an amide bond by treating a desired acid, Structure 13-5, with a desired amine according to methods known in the art. For example, a compound of Formula I can be prepared by treating Structure 13-5 with a desired amine R¹NH₂ in the presence of a base such as, for example, triethylamine, a coupling agent, for example, TBTU, and an organic solvent, for example, DMF. A compound of Formula I can optionally be treated with an organic acid, for example trifluoroacetic acid, and an organic solvent, for example, dichloromethane to remove a protecting group, for example, a Boc protecting group. This chemistry is illustrated in Scheme 13.

Scheme 14 illustrates a general procedure for preparing a compound of the present invention. Structure 14-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 14-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about room temperature. Structure 14-2 can be prepared by treating Structure 14-1 with a desired amine, R¹⁰R¹²NH, in the presence of a base such as, for example, diisopropylethylamine, and a mixture of organic solvents such as, for example, 2-propanol and dichloromethane at about 0° C. to about 25° C. for about 18 hours. The R¹² group can comprise an amino acid moiety that can comprise a protected amine that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. A compound of Structure 14-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 14-3 can be prepared by treating Structure 14-2 with a desired amine, for example, R⁹R¹³NH, a base and a mixture of organic solvents at about 45° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the mixture of organic solvents comprises 2-propanol and DMF. Structure 14-3 can be cyclized by amide bond formation by treating an amine with an acid according to methods known in the art. For example, a compound of Structure 14-3 can be treated with a coupling reagent, for example, O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU), a base, for example, triethylamine, and a mixture of organic solvents, for example DMF and dichloromethane. Structure 14-5 can be prepared by treatment of a desired ester with a desired base according to methods known in the art. For example, Structure 14-5 can be prepared by treating Structure 14-4 with a base such as lithium hydroxide and a mixture of solvents comprising water and tetrahydrofuran. A compound of Formula III can be prepared by forming an amide bond by treating a desired acid, Structure 14-5, with a desired amine according to methods known in the art. For example, a compound of Formula III can be prepared by treating Structure 14-5 with a desired amine R¹¹R¹⁴NH in the presence of a base such as, for example, triethylamine, a coupling agent, for example, TBTU, and an organic solvent, for example, DMF. A compound of Formula III can optionally be treated with an organic acid, for example trifluoroacetic acid, and an organic solvent, for example, dichloromethane to remove a protecting group, for example, a Boc protecting group. This chemistry is illustrated in Scheme 14.

Scheme 15 illustrates a general procedure for preparing a compound of the present invention. Structure 15-1 can be prepared by amination of a desired 5-substituted carbonyl chloride pyrimidine with a desired amine according to methods known in the art. For example, Structure 15-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired amine R¹—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. Structure 15-2 can be prepared by treating Structure 15-1 with a desired amine, R²—NH₂, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. to about 25° C. for about 18 hours. Compounds of Structure 15-3 can be prepared by amination of a desired 2-chloropyrimidine, Structure 15-2, with a desired amine according to methods known in the art. For example compounds of Structure 15-3 can be prepared by treating Structure 15-2 with a desired amine, for example, R³—NH₂, a base and an organic solvent at an elevated temperature. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. Compounds of Formula I can be prepared by treating a compound of Structure 15-3 with an oganometallic catalyst, a quinone, and an organic solvent according to methods known in the art. For example, Structure 15-3 can be treated with Grubb's 2^(nd) generation catalyst, a quinone, for example, benzoquinone, and an organic solvent, for example, toluene at an elevated temperature overnight. The compound of Formula I can optionally be treated with palladium on carbon under a hydrogen atmosphere in the presence of an organic solvent, for example, methanol to reduce an alkene to an alkane. This chemistry is illustrated in Scheme 15.

Scheme 16 illustrates a general procedure for preparing a compound of the present invention. Structure 16-1 can be prepared by amination of a desired 5-substituted carbonyl chloride pyrimidine with a desired amine according to methods known in the art. For example, Structure 16-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired amine R¹¹R¹⁴NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. Structure 16-2 can be prepared by treating Structure 16-1 with a desired amine, R¹⁰R¹²NH, in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. to about 25° C. for about 18 hours. Compounds of Structure 16-3 can be prepared by amination of a desired 2-chloropyrimidine, Structure 16-2, with a desired amine according to methods known in the art. For example compounds of Structure 16-3 can be prepared by treating Structure 16-2 with a desired amine, for example, R⁹R¹³NH, a base and an organic solvent at an elevated temperature. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. Compounds of Formula III can be prepared by treating a compound of Structure 16-3 with an oganometallic catalyst, a quinone, and an organic solvent according to methods known in the art. For example, Structure 16-3 can be treated with Grubb's 2^(nd) generation catalyst, a quinone, for example, benzoquinone, and an organic solvent, for example, toluene at an elevated temperature overnight. The compound of Formula III can optionally be treated with a catalyst for example, palladium on carbon under a hydrogen atmosphere in the presence of an organic solvent, for example, methanol to reduce an alkene to an alkane. This chemistry is illustrated in Scheme 16.

Scheme 17 illustrates a general procedure for preparing a compound of the present invention. Structure 17-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 17-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. The R² group can comprise an amino acid moiety that can have a protected amine that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Structure 17-2 can be prepared by treating Structure 17-1 with a desired amine, R³—NH₂, in an organic solvent such as, for example, dimethyl sulfoxide, at about 100° C. for about two hours. Structure 17-2 can be cyclized by amide bond formation by treating an amine with an acid according to methods known in the art. For example, a compound of Structure 17-2 can be treated with a coupling reagent, for example, [dimethylamino(triazolo[4,5-b]pyridin-3-yloxy)methylidene]-dimethylazanium hexafluoro-phosphate (HATU), a base, for example, diisopropylethylamine, and an organic solvent, for example DMF. Structure 17-3 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 17-4 can be prepared by treating Structure 17-3 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in an organic solvent at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the organic solvent is N,N-dimethylformamide. Structure 17-5 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 17-5 can be prepared by treating Structure 17-4 with a desired acid and solvents. In one embodiment, the acid is p-toluenesulfonic acid. In one embodiment, the solvents comprise water and acetone. Compounds of Formula II can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula II can be prepared by treating Structure 17-5 with a desired amine, for example, morpholine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. The compound of Formula II can optionally be treated with an organic acid, for example, trifluoroacetic acid, in the presence of an organic solvent, for example, dichloromethane to remove a protecting group, for example, a Boc protecting group.

In an alternate embodiment, Structure 17-5 can be oxidized by treating Structure 17-5 with a desired oxidizing agent according to methods known in the art. For example, Structure 17-5 can be treated with an oxidizing agent, for example, sodium chlorite, a phosphate, for example, monosodium phosphate, an alkene, for example, 2-methyl-2-butene and an organic solvent, for example, tert-butanol. The reaction can be quenched according to methods known in the art. For example, the reaction can be diluted with saturated aqueous sodium thiosulfate and diluted with aqueous hydrochloric acid to adjust the pH to 4.

A compound of Formula II can be prepared by forming an amide bond by treating a desired acid, Structure 17-6, with a desired amine according to methods known in the art. For example, a compound of Formula II can be prepared by treating Structure 17-6 with a desired amine, a coupling agent, for example, HATU, and an organic solvent, for example, DMF. A compound of Formula II can optionally be treated with an organic acid, for example trifluoroacetic acid, and an organic solvent, for example, dichloromethane to remove a protecting group, for example, a Boc protecting group. This chemistry is illustrated in Scheme 17.

Scheme 18 illustrates a general procedure for preparing a compound of the present invention. Structure 18-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 18-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. The R¹² group can comprise an amino acid moiety that can have a protected amine that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Structure 18-2 can be prepared by treating Structure 18-1 with a desired amine, R⁹R¹³NH, in an organic solvent such as, for example, dimethyl sulfoxide, at about 100° C. for about two hours. Structure 18-2 can be cyclized by amide bond formation by treating an amine with an acid according to methods known in the art. For example, a compound of Structure 18-2 can be treated with a coupling reagent, for example, [dimethylamino(triazolo[4,5-b]pyridin-3-yloxy)methylidene]-dimethylazanium hexafluoro-phosphate (HATU), a base, for example, diisopropylethylamine, and an organic solvent, for example DMF. Structure 18-3 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 18-4 can be prepared by treating Structure 18-3 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in an organic solvent at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the organic solvent is N,N-dimethylformamide. Structure 18-5 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 18-5 can be prepared by treating Structure 18-4 with a desired acid and solvents. In one embodiment, the acid is p-toluenesulfonic acid. In one embodiment, the solvents comprise water and acetone. Compounds of Formula IV can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula IV can be prepared by treating Structure 18-5 with a desired amine, for example, morpholine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. The compound of Formula IV can optionally be treated with an organic acid, for example, trifluoroacetic acid, in the presence of an organic solvent, for example, dichloromethane to remove a protecting group, for example, a Boc protecting group.

In an alternate embodiment, Structure 18-5 can be oxidized by treating Structure 18-5 with a desired oxidizing agent according to methods known in the art. For example, Structure 18-5 can be treated with an oxidizing agent, for example, sodium chlorite, a phosphate, for example, monosodium phosphate, an alkene, for example, 2-methyl-2-butene and an organic solvent, for example, tert-butanol. The reaction can be quenched according to methods known in the art. For example, the reaction can be diluted with saturated aqueous sodium thiosulfate and diluted with aqueous hydrochloric acid to adjust the pH to 4. A compound of Formula IV can be prepared by forming an amide bond by treating a desired acid, Structure 18-6, with a desired amine according to methods known in the art. For example, a compound of Formula IV can be prepared by treating Structure 18-6 with a desired amine, a coupling agent, for example, HATU, and an organic solvent, for example, DMF. A compound of Formula IV can optionally be treated with an organic acid, for example trifluoroacetic acid, and an organic solvent, for example, dichloromethane to remove a protecting group, for example, a Boc protecting group. This chemistry is illustrated in Scheme 18.

Scheme 19 illustrates a general procedure for preparing a compound of the present invention. Structure 19-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 19-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. The R² group can comprise a protected alcohol moiety that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Structure 19-2 can be prepared by treating Structure 19-1 with a desired amine, R³—NH₂, in an organic solvent such as, for example, dimethyl sulfoxide, at about 110° C. for about sixteen hours. Structure 19-2 can be cyclized by methods known in the art. For example, Structure 19-3 can be prepared by treating Structure 19-2 with an organometallic catalyst, a quinone, and an organic solvent according to methods known in the art. For example, Structure 19-2 can be treated with Greyla's catalyst, a quinone, for example, benzoquinone, and an organic solvent, for example, toluene at an elevated temperature overnight. Structure 19-3 can be coupled with a desired organotin reagent according to methods known in the art. For example, compounds of Formula II can be prepared by treating Structure 19-3 with a tin compound, copper chloride, lithium chloride, and an organometallic reagent in an organic solvent at an elevated temperature under an inert atmosphere. In one embodiment, the organometallic reagent is tetrakis(triphenylphosphine)palladium(0) (Pd(PPh₃)₄. In one embodiment, the organic solvent is dimethyl sulfoxide. Compounds of Formula II can be deprotected according to methods known in the art. For example compounds of Formula II comprising an alcohol protecting group, can be treated with an acid, for example, 10% concentrated hydrochloric acid and an organic solvent. In one embodiment, the organic solvent is dichloromethane. Compounds of Formula II can optionally be treated with a catalyst, hydrogen gas, an acid and an organic solvent to reduce an alkene to an alkane. In one embodiment, the catalyst is palladium on carbon. In one embodiment, the acid is acetic acid. In one embodiment, the organic solvent is methanol. This chemistry is illustrated in Scheme 19.

Scheme 20 illustrates a general procedure for preparing a compound of the present invention. Structure 20-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 20-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. The R¹² group can comprise a protected alcohol moiety that can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Structure 20-2 can be prepared by treating Structure 20-1 with a desired amine, R⁹R¹³NH, in an organic solvent such as, for example, dimethyl sulfoxide, at about 110° C. for about sixteen hours. Structure 20-2 can be cyclized by methods known in the art. For example, Structure 20-3 can be prepared by treating Structure 20-2 with an organometallic catalyst, a quinone, and an organic solvent according to methods known in the art. For example, Structure 20-2 can be treated with Greyla's catalyst, a quinone, for example, benzoquinone, and an organic solvent, for example, toluene at an elevated temperature overnight. Structure 20-3 can be coupled with a desired organotin reagent according to methods known in the art. For example, compounds of Formula IV can be prepared by treating Structure 20-3 with a tin compound, copper chloride, lithium chloride, and an organometallic reagent in an organic solvent at an elevated temperature under an inert atmosphere. In one embodiment, the organometallic reagent is tetrakis(triphenylphosphine)palladium(0) (Pd(PPh₃)₄. In one embodiment, the organic solvent is dimethyl sulfoxide. Compounds of Formula IV can be deprotected according to methods known in the art. For example compounds of Formula IV comprising an alcohol protecting group, can be treated with an acid, for example, 10% concentrated hydrochloric acid and an organic solvent. In one embodiment, the organic solvent is dichloromethane. Compounds of Formula IV can optionally be treated with a catalyst, hydrogen gas, an acid and an organic solvent to reduce an alkene to an alkane. In one embodiment, the catalyst is palladium on carbon. In one embodiment, the acid is acetic acid. In one embodiment, the organic solvent is methanol. This chemistry is illustrated in Scheme 20.

Scheme 21 illustrates a general procedure for preparing a compound of the present invention. Structure 21-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 21-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. The R² group can comprise an alkene moiety and a protected alcohol moiety. The protected alcohol can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Structure 21-2 can be prepared by treating Structure 21-1 with a desired amine, R³—NH₂, in an organic solvent such as, for example, dimethyl sulfoxide, at about 100° C. for about two hours. The R³—NH₂ amine can comprise an alkene moiety. Structure 21-2 can be cyclized by carbon-carbon bond formation by treating an alkene with an alkene according to methods known in the art. For example, Structure 21-2 can be treated with Grubb's 2^(nd) generation catalyst, a quinone, for example, benzoquinone, and an organic solvent, for example, toluene at an elevated temperature overnight Structure 21-3 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 21-4 can be prepared by treating Structure 21-3 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in an organic solvent at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the organic solvent is N,N-dimethylformamide. Structure 21-5 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 21-5 can be prepared by treating Structure 21-4 with a desired acid and solvents. In one embodiment, the acid is p-toluenesulfonic acid. In one embodiment, the solvents comprise water and acetone. It should be noted that a protected alcohol can simultaneously be deprotected under these conditions. Compounds of Formula II can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula II can be prepared by treating Structure 21-5 with a desired amine, for example, morpholine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. This chemistry is illustrated in Scheme 21.

Scheme 22 illustrates a general procedure for preparing a compound of the present invention. Structure 22-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 22-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R¹⁰R¹²NH in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. The R¹² group can comprise an alkene moiety and a protected alcohol moiety. The protected alcohol can be deprotected at a later step. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. Structure 22-2 can be prepared by treating Structure 22-1 with a desired amine, R⁹R¹³NH, in an organic solvent such as, for example, dimethyl sulfoxide, at about 100° C. for about two hours. The R⁹R¹³NH amine can comprise an alkene moiety. Structure 22-2 can be cyclized by carbon-carbon bond formation by treating an alkene with an alkene according to methods known in the art. For example, Structure 22-2 can be treated with Grubb's 2^(nd) generation catalyst, a quinone, for example, benzoquinone, and an organic solvent, for example, toluene at an elevated temperature overnight. Structure 22-3 can be coupled with a desired borane reagent according to methods known in the art. For example, Structure 22-4 can be prepared by treating Structure 22-3 with a trihydroxyborate lithium reagent, copper bromide, a base, and an organometallic reagent in an organic solvent at an elevated temperature. In one embodiment, the base is potassium carbonate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)). In one embodiment, the organic solvent is N,N-dimethylformamide. Structure 22-5 can be prepared by treating a desired 1,3-dioxolane with an acid according to methods known in the art. For example, Structure 22-5 can be prepared by treating Structure 22-4 with a desired acid and solvents. In one embodiment, the acid is p-toluenesulfonic acid. In one embodiment, the solvents comprise water and acetone. It should be noted that a protected alcohol can simultaneously be deprotected under these conditions. Compounds of Formula IV can be prepared by reductive amination of a desired aldehyde with a desired amine and a reducing agent according to methods known in the art. For example compounds of Formula IV can be prepared by treating Structure 22-5 with a desired amine, for example, morpholine, a reducing agent, for example, sodium trioxyacetylborohydride, an organic solvent and an acid. In one embodiment, the organic solvent is dichloromethane. In one embodiment, the acid is acetic acid. This chemistry is illustrated in Scheme 22.

Scheme 23 illustrates a general procedure for preparing a compound of the present invention. Structure 23-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 23-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about room temperature. Structure 23-2 can be prepared by treating Structure 23-1 with a desired amine, R²—NH₂, for example, 2-(2-aminoethoxyl)ethanol, in the presence of a base such as, for example, diisopropylethylamine, and an organic solvent such as, for example, 2-propanol at about 0° C. for about 1.5 hours. The R² group can comprise an alcohol moiety. The alcohol moiety can be protected according to methods known in the art. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. A compound of Structure 23-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 23-3 can be prepared by treating Structure 23-2 with a desired amine, for example, R³—NH₂, a base and an organic solvent at about 25° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. In one embodiment, the R³—NH₂ comprises an alcohol group. Structure 23-3 can be cyclized by ether bond formation according to methods known in the art. For example, a compound of Structure 23-3 comprising an alcohol group on the R³ moiety can be treated with organic reagents to activate the alcohol as a leaving group according to methods known in the art. For example, the alcohol can be treated with methanesulfonyl chloride, a base, for example, diisopropylethylamine and an organic solvent, for example, dichloromethane. The R² group comprising a protected alcohol moiety can be deprotected according to methods known in the art. It should be noted that upon deprotection, an ether macrocycle is generated. Structure 23-5 can be prepared by treatment of a desired ester with a desired base according to methods known in the art. For example, Structure 23-5 can be prepared by treating Structure 23-4 with a base such as 4.0 molar potassium hydroxide and an organic solvent, for example, methanol. A compound of Formula I can be prepared by forming an amide bond by treating a desired acid, Structure 23-5, with a desired amine according to methods known in the art. For example, a compound of Formula I can be prepared by treating Structure 23-5 with a desired amine R¹NH₂ in the presence of a base such as, for example, diisopropylethylamine, a coupling agent, for example, HATU, and an organic solvent, for example, DMF. This chemistry is illustrated in Scheme 23.

Scheme 24 illustrates a general procedure for preparing a compound of the present invention. Structure 24-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 24-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. to about room temperature. Structure 24-2 can be prepared by treating Structure 24-1 with a desired amine, R¹⁰R¹²NH, for example, 2-(2-aminoethoxyl)ethanol, in the presence of a base such as, for example, diisopropylethylamine, and an organic solvent such as, for example, 2-propanol at about 0° C. for about 1.5 hours. The R¹² group can comprise an alcohol moiety. The alcohol moiety can be protected according to methods know in the art. The protection and deprotection of functional groups such as amines and alcohols is well known to those skilled in the art. See, for example, Green, T. W. and Wuts, P. G. M. Protective Groups in Organic Synthesis, 2^(nd) Ed., John Wiley and Sons, Inc. New York, 1991. A compound of Structure 24-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 24-3 can be prepared by treating Structure 24-2 with a desired amine, for example, R⁹R¹³NH, a base and an organic solvent at about 25° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is 2-propanol. In one embodiment, the R⁹R¹³NH comprises an alcohol group. Structure 24-3 can be cyclized by ether bond formation according to methods known in the art. For example, a compound of Structure 24-3 comprising an alcohol group on the R¹³ moiety can be treated with organic reagents to activate the alcohol as a leaving group according to methods known in the art. For example, the alcohol can be treated with methanesulfonyl chloride, a base, for example, diisopropylethylamine and an organic solvent, for example, dichloromethane. The R¹² group comprising a protected alcohol moiety can be deprotected according to methods known in the art. It should be noted that upon deprotection, an ether macrocycle is generated. Structure 24-5 can be prepared by treatment of a desired ester with a desired base according to methods know in the art. For example, Structure 24-5 can be prepared by treating Structure 234-4 with a base such as 4.0 molar potassium hydroxide and an organic solvent, for example, methanol. A compound of Formula III can be prepared by forming an amide bond by treating a desired acid, Structure 24-5, with a desired amine according to methods known in the art. For example, a compound of Formula III can be prepared by treating Structure 24-5 with a desired amine R¹¹R¹⁴NH in the presence of a base such as, for example, diisopropylethylamine, a coupling agent, for example, HATU, and an organic solvent, for example, DMF. This chemistry is illustrated in Scheme 24.

Scheme 25 illustrates a general procedure for preparing a compound of the present invention. Structure 25-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 25-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. for about one hour. Structure 25-2 can be prepared by treating Structure 25-1 with a desired amine, R²—NH₂, for example, hex-5-yn-1-amine, in the presence of a base such as, for example, diisopropylethylamine, and an organic solvent such as, for example, ethanol at about 25° C. for about 3.5 hours. The R² group can comprise an alkyne moiety. Structure 25-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 25-3 can be prepared by treating Structure 25-2 with a desired amine, for example, R³—NH₂ (for example, 6-azidohexan-1-amine) and an organic solvent at about 50° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is ethanol. In one embodiment, Structure 25-3 can be cyclized by heteroaryl bond formation according to methods known in the art. For example, a compound of Structure 25-3 comprising an alkyne group on the R² group and an azide group on the R³ moiety can be treated with a tertiary amine, for example, tris(benzyltriazolylmethyl)amine (TBTA), and a copper compound, for example, Cu(MeCN)₄BF₄, and an organic solvent, for example, dichloromethane according to methods known in the art. In some embodiments, the reaction is carried out at an elevated temperature of about 45° C. for about 24 hours. Structure 25-5 can be prepared by treatment of a desired ester with a desired base according to methods known in the art. For example, Structure 25-5 can be prepared by treating Structure 25-4 with a base such as 10% aqueous potassium hydroxide and an organic solvent, for example, methanol. In some embodiments, the reaction is carried out at an elevated temperature of about 60° C. for about 12 hours. A compound of Formula I can be prepared by forming an amide bond by treating a desired acid, Structure 25-5, with a desired amine according to methods known in the art. For example, a compound of Formula I can be prepared by treating Structure 25-5 with a desired amine R¹NH₂ in the presence of a base such as, for example, diisopropylethylamine, a coupling agent, for example, HATU, and an organic solvent, for example, DMF. This chemistry is illustrated in Scheme 25.

Scheme 26 illustrates a general procedure for preparing a compound of the present invention. Structure 26-1 can be prepared by treatment of a desired 5-substituted carbonyl chloride pyrimidine with a desired alcohol according to methods known in the art. For example, Structure 26-1 can be prepared by treating a mixture of a commercially available 2,4-dichloropyrimidine-5-carbonyl chloride and a desired alcohol in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dichloromethane, at about 0° C. for about one hour. Structure 26-2 can be prepared by treating Structure 26-1 with a desired amine, R¹⁰R¹²NH, for example, hex-5-yn-1-amine, in the presence of a base such as, for example, diisopropylethylamine, and an organic solvent such as, for example, ethanol at about 25° C. for about 3.5 hours. The R¹² group can comprise an alkyne moiety. Structure 26-3 can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 26-3 can be prepared by treating Structure 26-2 with a desired amine, for example, R⁹R¹³NH (for example, 6-azidohexan-1-amine) and an organic solvent at about 50° C. In one embodiment, the base is diisopropylethylamine. In one embodiment, the organic solvent is ethanol. In one embodiment, Structure 26-3 can be cyclized by heteroaryl bond formation according to methods known in the art. For example, a compound of Structure 26-3 comprising an alkyne group on the R¹² group and an azide group on the R¹³ moiety can be treated with a tertiary amine, for example, tris(benzyltriazolylmethyl)amine (TBTA), and a copper compound, for example, Cu(MeCN)₄BF₄, and an organic solvent, for example, dichloromethane according to methods known in the art. In some embodiments, the reaction is carried out at an elevated temperature of about 45° C. for about 24 hours. Structure 26-5 can be prepared by treatment of a desired ester with a desired base according to methods known in the art. For example, Structure 26-5 can be prepared by treating Structure 26-4 with a base such as 10% aqueous potassium hydroxide and an organic solvent, for example, methanol. In some embodiments, the reaction is carried out at an elevated temperature of about 60° C. for about 12 hours. A compound of Formula III can be prepared by forming an amide bond by treating a desired acid, Structure 26-5, with a desired amine according to methods known in the art. For example, a compound of Formula III can be prepared by treating Structure 26-5 with a desired amine R¹¹R¹⁴NH in the presence of a base such as, for example, diisopropylethylamine, a coupling agent, for example, HATU, and an organic solvent, for example, DMF. This chemistry is illustrated in Scheme 26.

Scheme 27 illustrates a general procedure for preparing a compound of the present invention. Structure 27-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 27-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine R²—NH₂ in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 27-1 can be coupled with a desired borane reagent according to methods known in the art. For example, boronic acid, Structure 27-2 can be prepared by treating Structure 27-1 with a diborane reagent, a salt, and an organometallic reagent in an organic solvent at an elevated temperature. In one embodiment, the salt is potassium acetate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)₂). In one embodiment, the organic solvent is dioxane. The product, a diborane ester can be hydrolyzed to a boronic acid by treating the ester with an acid, for example, trifluoroacetic acid, in a mixture of solvents, for example, methanol and water. Structure 27-3 can be prepared by treating a desired boronic acid with a halide according to methods known in the art. For example, Structure 27-3 can be prepared by treating Structure 27-2 with a halide, a salt, an organometallic reagent, and a phosphine in an organic solvent at an elevated temperature. In one embodiment, the salt is tripotassium phosphate. In one embodiment, the organometallic reagent is tris(dibenzylideneacetone)dipalladium(0). In one embodiment, the phosphine is tricyclohexylphosphine (P(Cy)₃). In one embodiment, the organic solvent is dioxane. Compounds of Formula II can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, compounds of Formula II can be prepared by treating Structure 27-3 with a desired amine, for example, R³NH₂, optionally in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dimethyl sulfoxide, at about 110° C. for about 12 hours.

Scheme 28 illustrates a general procedure for preparing a compound of the present invention. Structure 28-1 can be prepared by amination of a desired 4-chloropyrimidine with a desired amine according to methods known in the art. For example, Structure 28-1 can be prepared by treating a mixture of a commercially available 5-bromo-2,4-dichloropyrimidine and a desired amine in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, 2-propanol, at about 0° C. Structure 28-1 can be coupled with a desired borane reagent according to methods known in the art. For example, boronic acid, Structure 28-2 can be prepared by treating Structure 28-1 with a diborane reagent, a salt, and an organometallic reagent in an organic solvent at an elevated temperature. In one embodiment, the salt is potassium acetate. In one embodiment, the organometallic reagent is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (PdCl₂(dppf)₂). In one embodiment, the organic solvent is dioxane. The product, a diborane ester can be hydrolyzed to a boronic acid by treating the ester with an acid, for example, trifluoroacetic acid, in a mixture of solvents, for example, methanol and water. Structure 28-3 can be prepared by treating a desired boronic acid with a halide according to methods known in the art. For example, Structure 28-3 can be prepared by treating Structure 28-2 with a halide, a salt, an organometallic reagent, and a phosphine in an organic solvent at an elevated temperature. In one embodiment, the salt is tripotassium phosphate. In one embodiment, the organometallic reagent is tris(dibenzylideneacetone)dipalladium(0). In one embodiment, the phosphine is tricyclohexylphosphine (P(Cy)₃). In one embodiment, the organic solvent is dioxane. Compounds of Formula IV can be prepared by amination of a desired 2-chloropyrimidine with a desired amine according to methods known in the art. For example, compounds of Formula IV can be prepared by treating Structure 28-3 with a desired amine, for example, R⁹R¹³NH, optionally in the presence of a base such as, for example, diisopropylethylamine, in an organic solvent such as, for example, dimethyl sulfoxide, at about 110° C. for about 12 hours.

Compounds of Formula I, Formula II, Formula III or Formula IV can be metabolized to generate pyrimidine compounds. For example, a compound of Formula I, Formula II, Formula III or Formula IV can be dealkylated at the two position to generate a 2-aminopyrimidine, see below. In another embodiment, a compound of Formula I, Formula II, Formula III or Formula IV comprising a methylated amine can be demethylated to generate a compound of Formula I, Formula II, Formula III or Formula IV. In one embodiment, a compound of Formula I, Formula II, Formula III or Formula IV can be oxidized to generate a compound of Formula I, Formula II, Formula III or Formula IV. For example, a compound of Formula I, Formula II, Formula III or Formula IV comprising a heterocyclic ring containing a nitrogen atom at the R¹, R¹¹ or R¹⁹ position can be oxidized to generate an N-oxide of Formula I, Formula II, Formula III or Formula IV. In another embodiment, a compound of Formula I, Formula II, Formula III or Formula IV comprising a piperazine group can be oxidized twice to generate a piperazine bis-N-oxide of Formula I, Formula II, Formula III or Formula IV. In another embodiment, a compound of Formula I, Formula II, Formula III or Formula IV can be oxidized to generate a pyrimidine N-oxide, for example, as illustrated in Scheme 29.

Example 2 2-(Butylamino)-4-((1r,4r)-4-hydroxycyclohexyl)amino)-N-(4-(morpholino-sulfonyl)phenyl)pyrimidine-5-carboxamide General Procedure A:

2,4-Dichloro-N-(4-(morpholinosulfonyl)phenyl)pyrimidine-5-carboxamide

A solution of 2,4-dichloropyrimidine-5-carbonyl chloride (422 mg, 2.0 mmol) in dichloromethane (10 mL) was added 4-(morpholinosulfonyl)aniline (508 mg, 2.1 mmol) and DIEA (387 mg, 3.0 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 1 h. Then, water was added. The resulting mixture was extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄), filtered and concentrated. The residue was purified on ISCO to give the title compound as a white solid (701.2 mg, 84%). ¹H NMR (400 MHz, DMSO-d⁶) δ 11.98-11.90 (m, 1H), 8.29 (d, J=6.4 Hz, 1H), 7.89 (d, J=8.8 Hz, 2H), 7.69 (d, J=8.8 Hz, 2H), 3.65-3.56 (m, 4H), 2.87-2.78 (m, 4H); MS m/z 418.30 [M+H]⁺.

2-Chloro-4-(((1r,4r)-4-hydroxycyclohexyl)amino)-N-(4-(morpholinosulfonyl)phenyl) pyrimidine-5-carboxamide

A solution of 2,4-dichloro-N-(4-(morpholinosulfonyl)phenyl)pyrimidine-5-carboxamide (700 mg, 1.68 mmol) in IPA (15 mL) was added trans-4-aminocyclohexanol (231.4 mg, 2.2 mmol) and DIEA (387 mg, 3.0 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 50 min and warmed to room temperature and stirred for another 50 min. Then the solvent was removed, the residue was dissolved in a mixture of DCM and methanol (20 mL, 3:2, v/v), the suspension was filtered though a filter paper to give the title compound as a white solid (683.4 mg, 82%). ¹H NMR (400 MHz, DMSO-d⁶) δ 10.71 (s, 1H), 8.69 (s, 1H), 7.96-7.89 (m, 2H), 7.76-7.70 (m, 2H), 4.57 (s, 1H), 3.93-3.81 (m, 1H), 3.64-3.57 (m, 4H), 3.49-3.40 (m, 1H), 2.88-2.78 (m, 4H), 1.95-1.86 (m, 2H), 1.85-1.76 (m, 2H), 1.38-1.20 (m, 4H); MS m/z 496.20 [M+H]⁺.

2-(Butylamino)-4-(((1r,4r)-4-hydroxycyclohexyl)amino)-N-(4-(morpholinosulfonyl)phenyl)pyrimidine-5-carboxamide

A solution of 2-chloro-4-(((1r,4r)-4-hydroxycyclohexyl)amino)-N-(4-(morpholinosulfonyl)phenyl) pyrimidine-5-carboxamide (86 mg, 0.17 mmol) in IPA (10 mL) was added butylamine (59.6 mg, 0.81 mmol) and DIEA (124.7 mg, 0.96 mmol) at room temperature. The resulting mixture was stirred for 3 h at room temperature. Water was then added. The resulting mixture was extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄), filtered and concentrated. The residue was purified on ISCO to give the title compound as a white solid (59.3 mg, 64%). ¹H NMR (400 MHz, CD₃OD+CDCl₃) δ 8.21 (s, 1H), 7.71-7.64 (m, 2H), 7.59-7.53 (m, 2H), 3.93-3.77 (m, 1H), 3.74-3.64 (m, 4H), 3.63-3.58 (m, 4H), 3.56-3.46 (m, 1H), 3.26 (t, J=7.1 Hz, 2H), 2.91-2.81 (m, 4H), 2.05-1.95 (m, 2H), 1.93-1.82 (m, 2H), 1.50-1.41 (m, 2H), 1.33-1.17 (m, 6H), 0.83 (t, J=7.3 Hz, 3H); ¹³C NMR (101 MHz, CD₃OD+CDCl₃) δ 166.8, 156.4, 143.5, 128.8, 128.6, 120.3, 120.2, 69.2, 66.0, 45.9, 41.0, 33.4, 31.6, 30.2, 20.0, 13.7; MS m/z 533.30 [M+H]⁺.

Table 2 describes compounds prepared following procedures described in Example 2 (General Procedure A), using appropriate reagents. (Note: MerTK IC50. ++++ means <10 nM; +++ means between 10-100 nM, ++ means between 100 nM-1 μM; + means between 1-30 μM; − means inactive.)

Mer Physical Data MS m/z Structure Compound_ID IC₅₀ (M + 1) or/and ¹H NMR  1

UNC1817A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.27 (s, 1H), 7.85 (d, J = 8.4 Hz, 2H), 7.47 (d, J = 8.4 Hz, 2H), 4.52 (s, 2H), 4.00-3.91 (m, 1H), 3.63-3.55 (m, 1H), 3.36 (t, J = 6.9 Hz, 2H), 2.10 (d, J = 11.0 Hz, 2H), 1.97 (d, J = 10.4 Hz, 2H), 1.59 (dt, J = 15.0, 7.3 Hz, 2H), 1.47-1.25 (m, 6H), 0.97 (t, J = 7.4 Hz, 3H); MS m/z 477.25 [M + H]⁺.  2

UNC1819A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.39 (s, 1H), 7.64-7.53 (m, 2H), 7.14- 7.03 (m, 2H), 4.12-4.01 (m, 1H), 3.67-3.59 (m, 1H), 3.55-3.39 (m, 2H), 2.16- 2.06 (m, 2H), 2.05-1.94 (m, 2H), 1.71-1.61 (m, 2H), 1.54-1.35 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 402.30 [M + H]⁺.  3

UNC1820A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.40 (s, 1H), 7.64-7.57 (m, 2H), 7.13- 7.04 (m, 2H), 3.58-3.40 (m, 4H), 3.11-3.02 (m, 1H), 2.08 (d, J = 10.3 Hz, 2H), 1.95 (d, J = 12.0 Hz, 2H), 1.73 (s, 1H), 1.70-1.61 (m, 2H), 1.49-1.34 (m, 4H), 1.29-1.15 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 415.30 [M + H]⁺.  4

UNC1855A ++++ ¹H NMR (400 MHz, CDCl₃) δ 9.58 (d, J = 7.43 Hz, 1H), 8.04 (s, 1H), 3.97 (d, J = 12.7 Hz, 2H), 3.82-3.80 (m, 6H), 3.56-3.47 (m, 1H), 3.33-3.25 (m, 3H), 2.70 (t, J = 11.8 Hz, 1H), 2.00-1.94 (m, 2H), 1.92- 1.84 (m, 2H), 1.80-1.69 (m, 2H), 1.54-1.44 (m, 2H), 1.35-1.23 (m, 16H), 0.82 (t, J = 7.4 Hz, 3H); MS m/z 491.40 [M + H]⁺.  5

UNC1856A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.73 (t, J = 5.6 Hz, 1H), 7.83 (d, J = 7.4 Hz, 1H), 7.54 (s, 1H), 4.46 (d, J = 7.8 Hz, 1H), 4.10 (d, J = 13.6 Hz, 2H), 4.01-3.90 (m, 1H), 3.75-3.62 (m, 2H), 3.45-3.35 (m, 2H), 3.05 (t, J = 11.9 Hz, 2H), 2.13-1.96 (m, 9H), 1.66-1.57 (m, 2H), 1.43 (s, 9H), 1.41-1.33 (m, 6H), 0.93 (t, J = 7.4 Hz, 3H); MS m/z 491.35 [M + H]⁺.  6

UNC1857A ++++ ¹H NMR (400 MHz, CDCl₃) δ 8.30 (s, 1H), 8.07 (s, 1H), 7.67 (s, 4H), 5.28 (s, 1H), 3.94 (s, 1H), 3.74- 3.65 (m, 4H), 3.37 (dd, J = 13.1, 6.6 Hz, 2H), 3.03- 2.89 (m, 4H), 2.78-2.63 (m, 1H), 2.14-2.01 (m, 2H), 1.88 (d, J = 10.2 Hz, 2H), 1.70 (s, 3H), 1.59-1.48 (m, 2H), 1.41-1.22 (m, 6H), 0.92 (t, J = 7.3 Hz, 3H); MS m/z 532.30 [M + H]⁺.  7

UNC1858A ++++ ¹H NMR (400 MHz, CDCl₃) δ 8.08 (s, 1H), 3.97-3.87 (m, 1H), 3.87- 3.75 (m, 1H), 3.59-3.50 (m, 4H), 3.29-3.23 (m, 4H), 2.78 (td, J = 12.6, 2.8 Hz, 2H), 2.04-1.86 (m, 6H), 1.80-1.66 (m, 2H), 1.50- 1.41 (m, 2H), 1.33-1.16 (m, 6H), 0.83 (t, J = 7.3 Hz, 3H); MS m/z 391.30 [M + H]⁺.  8

UNC1936A ++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.39 (s, 1H), 7.82 (d, J = 8.8 Hz, 2H), 7.72-7.65 (m, 2H), 4.20 (s, 4H), 4.07 (s, 1H), 3.75-3.67 (m, 4H), 3.66- 3.57 (m, 1H), 3.00 (s, 3H), 2.98-2.94 (m, 4H), 2.20- 2.05 (m, 2H), 2.04-1.93 (m, 2H), 1.48-1.34 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 153.3, 144.1, 142.4, 130.0, 128.8, 120.7, 100.3, 68.6, 66.0, 49.6, 45.9, 32.9, 29.5, 27.5; MS m/z 491.30 [M + H]⁺.  9

UNC1937A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.46 (s, 1H), 7.92-7.81 (m, 2H), 7.77-7.68 (m, 2H), 4.14- 4.02 (m, 1H), 3.76-3.66 (m, 4H), 3.68-3.59 (m, 1H), 3.51 (dd, J = 14.2, 7.0 Hz, 2H), 3.02-2.90 (m, 4H), 2.13 (d, J = 8.5 Hz, 2H), 2.00 (d, J = 9.1 Hz, 2H), 1.45 (dd, J = 18.7, 10.0 Hz, 4H), 1.28 (t, J = 7.2 Hz, 3H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 152.7, 144.4, 142.5, 130.0, 128.7, 120.5, 100.8, 68.4, 65.84, 49.7, 46.0, 36.3, 32.8, 29.3, 13.3; MS m/z 505.30 [M + H]⁺. 10

UNC1938A ++++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.90-7.82 (m, 2H), 7.75-7.68 (m, 2H), 4.12- 3.98 (m, 1H), 3.80-3.66 (m, 4H), 3.67-3.59 (m, 1H), 3.43 (t, J = 7.1 Hz, 2H), 3.03-2.91 (m, 4H), 2.22- 2.09 (m, 2H), 2.07-1.95 (m, 2H), 1.74-1.63 (m, 2H), 1.53-1.35 (m, 4H), 0.99 (t, J = 7.4 Hz, 3H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.3, 159.8, 153.2, 144.8, 142.6, 129.9, 128.7, 120.6, 100.6, 68.5, 65.9, 49.7, 46.00, 43.1, 32.8, 29.4, 22.0, 10.7; MS m/z 519.30 [M + H]⁺. 11

UNC1939A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.89-7.81 (m, 2H), 7.74-7.67 (m, 2H), 4.26- 4.15 (m, 1H), 4.13-4.02 (m, 1H), 3.75-3.68 (m, 4H), 3.68-3.60 (m, 1H), 3.00- 2.92 (m, 4H), 2.20-2.08 (m, 2H), 2.05-1.96 (m, 2H), 1.53-1.37 (m, 4H), 1.32 (s, 3H), 1.30 (s, 3H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 152.0, 144.5, 142.5, 130.0, 128.9, 128.7, 120.5, 117.5, 100.7, 68.4, 65.8, 49.7, 46.0, 44.03, 32.7, 29.3, 22.2, 21.1; MS m/z 519.30 [M + H]⁺. 12

UNC1940A ++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.47 (s, 1H), 7.89-7.83 (m, 2H), 7.75-7.71 (m, 2H), 4.12- 4.03 (m, 1H), 3.76 (t, J = 5.5 Hz, 2H), 3.74-3.68 (m, 4H), 3.68-3.57 (m, 3H), 3.00-2.93 (m, 4H), 2.16- 2.08 (m, 2H), 2.04-1.95 (m, 2H), 1.50-1.38 (m, 4H); 13C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.9, 153.0, 144.7, 142.5, 130.1, 128.7, 120.5, 100.9, 68.4, 65.8, 59.4, 49.6, 46.0, 43.6, 32.7, 29.3; MS m/z 521.20 [M + H]⁺. 13

UNC1941A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.40 (s, 1H), 7.83 (d, J = 8.8 Hz, 2H), 7.69 (d, J = 8.8 Hz, 2H), 4.08-3.99 (m, 1H), 3.74-3.68 (m, 4H), 3.68- 3.58 (m, 3H), 3.55 (t, J = 6.8 Hz, 2H), 3.01-2.90 (m, 4H), 2.15-2.04 (m, 2H), 2.04-1.93 (m, 2H), 1.89- 1.79 (m, 2H), 1.46-1.34 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 152.9, 144.2, 142.5, 129.9, 128.8, 120.7, 100.4, 68.5, 66.0, 59.2, 49.7, 45.9, 38.6, 32.8, 31.1, 29.5; MS m/z 535.30 [M + H]⁺. 14

UNC1942A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.43 (s, 1H), 7.86-7.77 (m, 2H), 7.74-7.65 (m, 2H), 7.34- 7.24 (m, 2H), 7.05-6.95 (m, 2H), 4.56 (s, 2H), 3.97-3.85 (m, 1H), 3.76-3.66 (m, 4H), 3.64-3.54 (m, 1H), 3.02- 2.90 (m, 4H), 2.03-1.88 (m, 4H), 1.43-1.26 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.1, 163.4, 161.0, 159.7, 152.8, 144.1, 142.4, 133.0, 130.0, 129.0, 128.9, 128.8, 120.8, 120.7, 115.48, 115.3, 100.8, 68.5, 66.0, 49.7, 45.9, 44.3, 33.0, 29.5; MS m/z 585.30 [M + H]⁺. 15

UNC1943A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.51- 8.46 (m, 1H), 7.87-7.79 (m, 2H), 7.73-7.65 (m, 2H), 7.64-7.55 (m, 2H), 7.42- 7.38 (m, 1H), 7.09-6.99 (m, 2H), 4.00-3.86 (m, 1H), 3.77-3.67 (m, 4H), 3.64- 3.56 (m, 1H), 3.03-2.91 (m, 4H), 2.15-2.05 (m, 2H), 2.05-1.92 (m, 2H), 1.45- 1.29 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 160.9, 160.4, 158.4, 142.8, 133.5, 129.6, 128.8, 122.9, 122.8, 120.6, 115.4, 115.2, 100.9, 68.7, 66.0, 49.8, 45.6, 33.2, 29.8; MS m/z 571.20 [M + H]⁺. 16

UNC1944A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.46 (s, 1H), 7.89-7.83 (m, 2H), 7.74-7.68 (m, 2H), 4.11- 4.02 (m, 1H), 3.74-3.68 (m, 4H), 3.67-3.60 (m, 1H), 3.57 (t, J = 6.8 Hz, 2H), 3.49 (t, J = 5.9 Hz, 2H), 3.35 (s, 3H), 3.00-2.93 (m, 4H), 2.18-2.07 (m, 2H), 2.07-1.98 (m, 2H), 1.95- 1.87 (m, 2H), 1.50-1.38 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 152.9, 144.5, 142.5, 130.0, 128.7, 120.6, 100.7, 70.1, 68.5, 65.9, 58.1, 49.7, 46.0, 39.0, 32.8, 29.4, 28.6; MS m/z 549.20 [M + H]⁺. 17

UNC1945A ++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.47 (s, 1H), 7.90-7.83 (m, 2H), 7.75-7.70 (m, 2H), 4.11- 4.01 (m, 1H), 4.01-3.92 (m, 2H), 3.76-3.67 (m, 4H), 3.67-3.58 (m, 1H), 3.47- 3.33 (m, 4H), 3.01-2.90 (m, 4H), 2.19-2.08 (m, 2H), 2.08-1.91 (m, 3H), 1.70 (d, J = 12.7 Hz, 2H), 1.56-1.30 (m, 6H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 153.3, 144.8, 142.5, 130.0, 128.7, 120.5, 100.9, 68.4, 67.3, 65.8, 49.8, 46.9, 46.0, 34.8, 32.9, 30.5, 29.3; MS m/z 575.30 [M + H]⁺. 18

UNC1946A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.88-7.81 (m, 2H), 7.75-7.67 (m, 2H), 4.11- 3.96 (m, 4H), 3.75-3.69 (m, 4H), 3.68-3.60 (m, 1H), 3.56-3.47 (m, 2H), 3.03- 2.92 (m, 4H), 2.16-2.07 (m, 2H), 2.05-1.94 (m, 4H), 1.80-1.64 (m, 2H), 1.51- 1.35 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.0, 159.8, 152.0, 144.1, 142.4, 130.1, 128.8, 120.7, 100.8, 68.3, 66.3, 65.9, 50.0, 46.0, 32.8, 31.8, 29.4; MS m/z 561.30 [M + H]⁺. 19

UNC1947A ++++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.87 (d, J = 8.8 Hz, 2H), 7.73 (d, J = 8.7 Hz, 2H), 4.08-3.98 (m, 1H), 3.90-3.82 (m, 1H), 3.75- 3.66 (m, 4H), 3.67-3.60 (m, 1H), 3.03-2.89 (m, 4H), 2.19-2.09 (m, 2H), 2.08- 1.94 (m, 4H), 1.90-1.78 (m, 2H), 1.69 (d, J = 12.1 Hz, 1H), 1.56-1.21 (m, 9H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.1, 159.7, 144.2, 142.5, 130.1, 128.7, 120.5, 100.9, 68.4, 65.8, 51.4, 50.1, 46.0, 32.9, 31.8, 29.3, 25.1, 24.7; MS m/z 559.30 [M + H]⁺. 20

UNC1948A + ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.58 (s, 1H), 7.90-7.81 (m, 2H), 7.74-7.64 (m, 2H), 4.04- 3.95 (m, 1H), 3.81 (s, 8H), 3.75-3.67 (m, 4H), 3.66- 3.59 (m, 1H), 3.03-2.86 (m, 4H), 2.16-2.05 (m, 2H), 2.05-1.94 (m, 2H), 1.50- 1.32 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.7, 159.6, 154.5, 147.9, 142.7, 129.7, 128.7, 120.7, 100.7, 68.5, 66.0, 65.9, 49.3, 46.0, 44.7, 32.8, 29.5; MS m/z 547.25 [M + H]⁺. 21

UNC1949A ++++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.89-7.80 (m, 2H), 7.76-7.68 (m, 2H), 7.26- 7.17 (m, 2H), 7.04-6.94 (m, 2H), 4.09-3.98 (m, 1H), 3.75-3.57 (m, 7H), 3.01- 2.88 (m, 6H), 2.19-2.08 (m, 2H), 2.07-1.97 (m, 2H), 1.53-1.36 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.1, 162.9, 160.5, 159.8, 152.9, 144.4, 142.5, 134.2, 130.1, 130.1, 130.0, 128.7, 120.6, 115.2, 115.0, 110.1, 100.9, 68.4, 65.9, 49.7, 46.0, 42.7, 34.2, 32.9, 29.4; MS m/z 599.25 [M + H]⁺. 22

UNC1950A ++++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (d, J = 1.9 Hz, 1H), 7.91-7.80 (m, 2H), 7.75-7.68 (m, 2H), 4.07 (dt, J = 8.9, 7.0 Hz, 1H), 3.76-3.67 (m, 4H), 3.67-3.58 (m, 1H), 3.46 (t, J = 6.7 Hz, 2H), 3.01-2.91 (m, 4H), 2.19-2.08 (m, 2H), 2.06-1.96 (m, 2H), 1.70- 1.61 (m, 2H), 1.52-1.30 (m, 10H), 0.95-0.84 (m, 3H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 153.0, 144.7, 142.6, 130.0, 128.7, 120.5, 109.9, 100.7, 68.4, 65.8, 49.7, 46.0, 41.4, 32.9, 31.3, 29.4, 28.7, 26.4, 22.3, 13.3; MS m/z 561.30 [M + H]⁺. 23

UNC1951A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.90-7.80 (m, 2H), 7.76-7.67 (m, 2H), 4.09- 3.98 (m, 1H), 3.77-3.66 (m, 4H), 3.67-3.59 (m, 1H), 3.28 (d, J = 6.8 Hz, 2H), 3.05-2.89 (m, 4H), 2.19- 2.08 (m, 2H), 2.05-1.90 (m, 3H), 1.53-1.34 (m, 4H), 0.99 (s, 3H), 0.97 (s, 3H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.4, 159.9, 153.9, 145.6, 142.6, 129.9, 128.7, 120.6, 100.6, 68.5, 65.9, 49.7, 46.0, 32.9, 29.4, 28.1, 19.5; MS m/z 533.30 [M + H]⁺. 24

UNC1952A ++++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.45 (s, 1H), 7.90-7.82 (m, 2H), 7.75-7.68 (m, 2H), 4.11- 4.03 (m, 1H), 3.76-3.67 (m, 4H), 3.67-3.56 (m, 3H), 3.50 (t, J = 6.9 Hz, 2H), 3.02-2.92 (m, 4H), 2.18- 2.08 (m, 2H), 2.07-1.96 (m, 2H), 1.78-1.68 (m, 2H), 1.66-1.56 (m, 2H), 1.54- 1.34 (m, 4H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 164.2, 159.8, 153.0, 144.7, 142.5, 130.0, 128.7, 120.6, 100.7, 68.4, 65.9, 61.2, 49.7, 46.00, 41.2, 32.8, 29.5, 29.4, 25.3; MS m/z 549.30 [M + H]⁺. 25

UNC2020A + ¹H NMR (400 MHz, CD₃OD) δ 8.35 (s, 1H), 7.77 (d, J = 8.8 Hz, 2H), 7.63 (dd, J = 9.1, 2.0 Hz, 2H), 4.17 (s, 4H), 3.99-3.87 (m, 1H), 3.74-3.62 (m, 8H), 3.60-3.46 (m, 3H), 2.97- 2.87 (m, 4H), 2.73-2.45 (m, 6H), 2.11-1.98 (m, 2H), 1.98-1.88 (m, 2H), 1.40- 1.25 (m, 4H); MS m/z 590.30 [M + H]⁺. 26

UNC2021A + ¹H NMR (400 MHz, CD₃OD) δ 8.50-8.45 (m, 1H), 7.89 (d, J = 8.7 Hz, 2H), 7.76 (d, J = 8.7 Hz, 2H), 4.16-4.07 (m, 1H), 3.73-3.67 (m, 4H), 3.66- 3.57 (m, 1H), 3.00-2.90 (m, 4H), 2.15-2.06 (m, 2H), 2.03-1.95 (m, 2H), 1.51- 1.36 (m, 4H); MS m/z 477.20 [M + H]⁺. 27

UNC2022A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.38 (s, 1H), 7.81-7.75 (m, 2H), 7.70- 7.62 (m, 2H), 7.33 (d, J = 1.3 Hz, 1H), 3.93 (t, J = 6.5 Hz, 3H), 3.72-3.63 (m, 4H), 3.60-3.50 (m, 1H), 3.36 (t, J = 6.7 Hz, 2H), 2.94 (s, 7H), 2.11-2.00 (m, 2H), 2.00-1.91 (m, 2H), 1.47- 1.29 (m, 4H); MS m/z 583.20 [M + H]⁺. 28

UNC2023A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.37 (d, J = 7.4 Hz, 1H), 8.34 (s, 1H), 7.78 (d, J = 8.3 Hz, 2H), 7.65 (d, J = 8.6 Hz, 2H), 4.01-3.95 (m, 1H), 3.72-3.63 (m, 4H), 3.63-3.52 (m, 1H), 3.46 (t, J = 7.2 Hz, 2H), 2.99-2.80 (m, 4H), 2.13-1.85 (m, 4H), 1.47 (dd, J = 14.3, 7.1 Hz, 2H), 1.43-1.28 (m, 4H), 0.72-0.58 (m, 1H), 0.46- 0.36 (m, 2H), 0.07-0.05 (m, 2H); MS m/z 545.30 [M + H]⁺. 29

UNC2027A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.40 (s, 1H), 7.79 (d, J = 8.7 Hz, 2H), 7.65 (d, J = 8.7 Hz, 2H), 4.06-3.93 (m, 1H), 3.71- 3.60 (m, 4H), 3.60-3.54 (m, 1H), 3.49 (t, J = 7.1 Hz, 2H), 2.98-2.85 (m, 4H), 2.23-2.11 (m, 2H), 2.10- 2.01 (m, 2H), 2.00-1.81 (m, 4H), 1.46-1.27 (m, 4H); MS m/z 487.25 [M + H]⁺. 30

UNC2084A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.49 (d, J = 1.8 Hz, 1H), 7.91 (dd, J = 8.8, 1.7 Hz, 2H), 7.78-7.71 (m, 2H), 3.74-3.65 (m, 4H), 3.63-3.55 (m, 2H), 3.51 (t, J = 6.5 Hz, 2H), 3.43 (d, J = 12.5 Hz, 2H), 3.05-2.88 (m, 6H), 2.12-1.93 (m, 3H), 1.70-1.59 (m, 2H), 1.59- 1.37 (m, 4H), 1.03-0.90 (m, 3H); MS m/z 532.30 [M + H]⁺. 31

UNC2085A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.48 (s, 1H), 7.91 (d, J = 8.8 Hz, 2H), 7.75 (d, J = 8.7 Hz, 2H), 3.80-3.65 (m, 4H), 3.60- 3.43 (m, 4H), 3.12-3.04 (m, 1H), 3.03-2.91 (m, 4H), 2.09 (d, J = 10.6 Hz, 2H), 1.95 (d, J = 11.9 Hz, 2H), 1.78-1.60 (m, 3H), 1.53- 1.34 (m, 4H), 1.31-1.12 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 546.30 [M + H]⁺. 32

UNC2086A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.56 (s, 1H), 7.95-7.86 (m, 2H), 7.82- 7.73 (m, 2H), 4.50-4.38 (m, 1H), 3.74-3.68 (m, 4H), 3.59-3.41 (m, 4H), 3.25- 3.14 (m, 2H), 3.01-2.93 (m, 4H), 2.41-2.27 (m, 2H), 1.95-1.80 (m, 2H), 1.73- 1.59 (m, 2H), 1.53-1.38 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 518.30 [M + H]⁺. 33

UNC2058A ++ ¹H NMR (400 MHz, CDCl₃ + CD₃OD) δ 9.98 (s, 1H), 9.41 (t, J = 5.5 Hz, 1H), 8.57 (s, 1H), 8.19 (t, J = 5.2 Hz, 1H), 7.79 (d, J = 8.8 Hz, 2H), 7.64 (d, J = 8.7 Hz, 2H), 3.72-3.63 (m, 4H), 3.50 (dd, J = 12.8, 6.7 Hz, 2H), 3.41-3.33 (m, 2H), 3.08-3.00 (m, 2H), 2.97-2.86 (m, 4H), 1.67- 1.59 (m, 2H), 1.59-1.51 (m, 2H), 1.48-1.41 (m, 2H), 1.41-1.25 (m, 14H), 0.88 (t, J = 7.3 Hz, 3H); MS m/z 634.40 [M + H]⁺. 34

UNC2059A +++ ¹H NMR (400 MHz, CDCl₃) δ 9.83-9.59 (m, 1H), 8.69-8.49 (m, 1H), 8.16-7.98 (m, 2H), 7.98- 7.83 (m, 2H), 4.25-4.11 (m, 7H), 3.96-3.87 (m, 3H), 3.80-3.69 (m, 2H), 3.68- 3.57 (m, 2H), 3.57-3.44 (m, 2H), 3.22-3.12 (m, 3H), 3.10-2.98 (m, 2H), 1.92- 1.75 (m, 5H), 1.67-1.52 (m, 5H), 1.25-0.97 (m, 3H); MS m/z 534.30 [M + H]⁺. 35

UNC2060A + ¹H NMR (400 MHz, CD₃OD) δ 8.29 (s, 1H), 7.94 (d, J = 8.8 Hz, 2H), 7.77 (d, J = 8.8 Hz, 2H), 4.14-3.97 (m, 3H), 3.92- 3.86 (m, 2H), 3.73-3.67 (m, 4H), 3.63-3.41 (m, 6H), 3.38-3.33 (m, 2H), 2.99- 2.91 (m, 4H), 1.66 (dt, J = 14.8, 7.3 Hz, 2H), 1.45 (dt, J = 15.0, 7.4 Hz, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 548.30 [M + H]⁺. 36

UNC2061A +++ ¹H NMR (400 MHz, CDCl₃) δ 9.93 (s, 1H), 9.53 (d, J = 13 Hz, 1H), 8.66 (s, 1H), 8.21 (t, J = 5.4 Hz, 1H), 7.83 (d, J = 8.7 Hz, 2H), 7.69 (d, J = 8.7 Hz, 2H), 4.33-4.24 (m, 1H), 4.04-3.97 (m, 2H), 3.77- 3.67 (m, 4H), 3.60-3.49 (m, 2H), 3.47-3.39 (m, 2H), 3.05-2.90 (m, 4H), 2.03 (d, J = 10.9 Hz, 2H), 1.75-1.64 (m, 2H), 1.65-1.57 (m, 2H), 1.45-1.33 (m, 2H), 0.94 (t, J = 7.3 Hz, 3H); MS m/z 519.25 [M + H]⁺. 37

UNC2062A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.80 (t, J = 5.9 Hz, 1H), 9.55 (s, 1H), 8.76 (s, 1H), 8.60 (t, J = 5.1 Hz, 1H), 7.77 (d, J = 8.7 Hz, 2H), 7.64 (d, J = 8.7 Hz, 2H), 4.13-4.03 (m, 2H), 3.98 (s, 4H), 3.76-3.69 (m, 4H), 3.44-3.35 (m, 4H), 3.02-2.88 (m, 5H), 1.61 (dt, J = 15.0, 7.3 Hz, 2H), 1.39 (dq, J = 14.8, 7.3 Hz, 2H), 0.95 (t, J = 7.3 Hz, 3H); MS m/z 548.30 [M + H]⁺. 38

UNC2063A ¹H NMR (400 MHz, CDCl₃) δ 9.98 (s, 1H), 8.48 (s, 1H), 7.86 (s, 1H), 7.83 (s, 2H), 7.71 (d, J = 8.7 Hz, 2H), 3.88 (t, J = 5.2 Hz, 4H), 3.76-3.70 (m, 4H), 3.63 (t, J = 5.2 Hz, 4H), 3.37 (dd, J = 12.9, 7.0 Hz, 2H), 3.32 (s, 6H), 3.02-2.94 (m, 4H), 1.58 (dt, J = 15.0, 7.5 Hz, 2H), 1.36 (dt, J = 14.9, 7.4 Hz, 2H), 0.90 (t, J = 7.3 Hz, 3H); MS m/z 551.30 [M + H]⁺. 39

UNC2064A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.06 (s, 1H), 9.69 (s, 1H), 8.60 (s, 1H), 8.38 (t, J = 5.3 Hz, 1H), 7.81 (d, J = 8.7 Hz, 2H), 7.65 (d, J = 8.7 Hz, 2H), 3.85-3.77 (m, 2H), 3.77- 3.69 (m, 8H), 3.69-3.61 (m, 2H), 3.40 (dd, J = 12.9, 6.9 Hz, 2H), 3.02-2.92 (m, 4H), 1.64-1.52 (m, 2H), 1.37 (dq, J = 14.5, 7.3 Hz, 2H), 0.92 (t, J = 7.3 Hz, 3H); MS m/z 523.25 [M + H]⁺. 40

UNC2065A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.23 (s, 1H), 9.55 (t, J = 5.6 Hz, 1H), 8.57 (s, 1H), 8.16 (t, J = 5.2 Hz, 1H), 7.84 (d, J = 8.7 Hz, 2H), 7.68 (d, J = 8.7 Hz, 2H), 3.77-3.67 (m, 4H), 3.43-3.33 (m, 4H), 3.02-2.93 (m, 4H), 2.01-1.87 (m, 1H), 1.69-1.52 (m, 2H), 1.46-1.31 (m, 2H), 1.03- 0.90 (m, 9H); MS m/z 491.25 [M + H]⁺. 41

UNC2066A + ¹H NMR (400 MHz, CDCl₃) δ 9.69 (s, 2H), 8.75 (s, 1H), 8.30 (t, J = 5.4 Hz, 1H), 7.83 (d, J = 8.7 Hz, 2H), 7.71 (d, J = 8.7 Hz, 2H), 4.72-4.64 (m, 1H), 3.80-3.67 (m, 5H), 3.59- 3.51 (m, 2H), 3.50-3.40 (m, 2H), 3.04-2.92 (m, 4H), 2.36-2.26 (m, 1H), 2.08- 1.98 (m, 1H), 1.67-1.59 (m, 2H), 1.47 (s, 9H), 1.43-1.35 (m, 2H), 0.94 (t, J = 7.3 Hz, 3H); MS m/z 604.30 [M + H]⁺. 42

UNC2067A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.75 (t, J = 5.8 Hz, 1H), 9.33 (s, 1H), 8.87 (s, 1H), 7.85 (d, J = 8.6 Hz, 2H), 7.71 (d, J = 8.7 Hz, 2H), 3.90-3.83 (m, 1H), 3.77-3.69 (m, 4H), 3.58- 3.41 (m, 4H), 3.13-2.82 (m, 6H), 2.80-2.63 (m, 1H), 1.96-1.84 (m, 2H), 1.77- 1.68 (m, 1H), 1.67-1.49 (m, 3H), 1.47-1.35 (m, 10H), 0.96 (t, J = 7.3 Hz, 3H); MS m/z 632.35 [M + H]⁺. 43

UNC2068A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.71 (s, 2H), 8.75 (s, 1H), 8.30 (t, J = 5.3 Hz, 1H), 7.83 (d, J = 8.7 Hz, 2H), 7.70 (d, J = 8.7 Hz, 2H), 4.68 (s, 1H), 3.81-3.67 (m, 5H), 3.60-3.50 (m, 2H), 3.48-3.39 (m, 2H), 3.05- 2.91 (m, 4H), 2.36-2.25 (m, 1H), 2.08-1.96 (m, 1H), 1.68-1.56 (m, 2H), 1.47 (s, 9H), 1.44-1.31 (m, 2H), 0.94 (t, J = 7.3 Hz, 3H); MS m/z 604.30 [M + H]⁺. 44

UNC2069A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.71 (t, J = 5.5 Hz, 1H), 9.52 (s, 1H), 8.68 (s, 1H), 8.04 (s, 1H), 7.87 (d, J = 8.7 Hz, 2H), 7.71 (d, J = 8.6 Hz, 2H), 3.79-3.64 (m, 6H), 3.53 (t, J = 5.7 Hz, 2H), 3.46 (dd, J = 12.8, 6.9 Hz, 2H), 3.39 (s, 3H), 3.07- 2.91 (m, 4H), 1.99-1.88 (m, 2H), 1.67-1.56 (m, 2H), 1.39 (dq, J = 14.6, 7.3 Hz, 2H), 0.94 (t, J = 7.3 Hz, 3H); MS m/z 507.20 [M + H]⁺. 45

UNC2070A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.99 (s, 1H), 9.42 (t, J = 6.0 Hz, 1H), 8.50 (s, 1H), 8.27 (s, 1H), 7.82 (d, J = 8.7 Hz, 2H), 7.70 (d, J = 8.6 Hz, 2H), 3.75-3.71 (m, 4H), 3.68 (t, J = 6.3 Hz, 2H), 3.58 (dd, J = 12.8, 6.6 Hz, 2H), 3.43 (dd, J = 13.0, 6.8 Hz, 2H), 3.05-2.91 (m, 4H), 1.75-1.68 (m, 2H), 1.66-1.57 (m, 4H), 1.54- 1.45 (m, 2H), 1.43-1.34 (m, 2H), 0.93 (t, J = 7.3 Hz, 3H); MS m/z 521.30 [M + H]⁺. 46

UNC2071A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.94 (s, 1H), 9.49 (t, J = 5.5 Hz, 1H), 8.64 (s, 1H), 8.14 (t, J = 5.4 Hz, 1H), 7.83 (d, J = 8.7 Hz, 2H), 7.69 (d, J = 8.7 Hz, 2H), 4.01-3.92 (m, 2H), 3.79-3.67 (m, 4H), 3.65- 3.56 (m, 2H), 3.48-3.34 (m, 4H), 3.05-2.90 (m, 4H), 1.68-1.55 (m, 6H), 1.45- 1.27 (m, 4H), 0.93 (t, J = 7.3 Hz, 3H); MS m/z 547.30 [M + H]⁺. 47

UNC2072A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.25 (s, 1H), 9.58 (t, J = 5.7 Hz, 1H), 8.59 (s, 1H), 8.20 (t, J = 5.4 Hz, 1H), 7.82 (d, J = 8.7 Hz, 2H), 7.68 (d, J = 8.7 Hz, 2H), 4.01 (dd, J = 11.3, 3.6 Hz, 2H), 3.81-3.62 (m, 4H), 3.54-3.29 (m, 6H), 3.07-2.87 (m, 4H), 1.98- 1.84 (m, 1H), 1.70-1.63 (m, 2H), 1.64-1.53 (m, 2H), 1.49-1.29 (m, 4H), 0.93 (t, J = 7.3 Hz, 3H); MS m/z 533.25 [M + H]⁺. 48

UNC2073A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.90 (s, 1H), 9.47 (s, 1H), 8.51 (s, 1H), 8.31- 8.20 (m, 1H), 7.84 (d, J = 8.4 Hz, 2H), 7.71 (d, J = 8.5 Hz, 2H), 3.82-3.65 (m, 4H), 3.52-3.29 (m, 4H), 3.10- 2.87 (m, 4H), 1.66-1.54 (m, 2H), 1.42-1.33 (m, 2H), 1.19-1.06 (m, 1H), 0.93 (t, J = 7.3 Hz, 3H), 0.70-0.58 (m, 2H), 0.36-0.27 (m, 2H); MS m/z 489.20 [M + H]⁺. 49

UNC2074A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.03 (s, 1H), 9.55 (t, J = 5.5 Hz, 1H), 8.55 (s, 1H), 8.22 (s, 1H), 7.85 (d, J = 8.5 Hz, 2H), 7.71 (d, J = 8.4 Hz, 2H), 3.80-3.71 (m, 4H), 3.71- 3.59 (m, 2H), 3.53-3.39 (m, 2H), 3.06-2.93 (m, 4H), 1.72-1.52 (m, 4H), 1.50- 1.30 (m, 2H), 1.02-0.87 (m, 3H), 0.80-0.67 (m, 1H), 0.58-0.45 (m, 2H), 0.17- 0.06 (m, 2H); MS m/z 503.30 [M + H]⁺. 50

UNC2075A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.08 (s, 1H), 9.48 (t, J = 5.5 Hz, 1H), 8.53 (s, 1H), 8.28 (t, J = 4.9 Hz, 1H), 7.82 (d, J = 8.7 Hz, 2H), 7.68 (d, J = 8.6 Hz, 2H), 3.76-3.69 (m, 6H), 3.65-3.57 (m, 2H), 3.47- 3.36 (m, 2H), 3.04-2.90 (m, 4H), 1.82-1.74 (m, 2H), 1.71-1.64 (m, 2H), 1.62- 1.54 (m, 2H), 1.43-1.33 (m, 2H), 0.93 (t, J = 7.3 Hz, 3H); MS m/z 507.30 [M + H]⁺. 51

UNC2092A + ¹H NMR (400 MHz, CDCl₃) δ 8.38 (s, 1H), 7.90-7.61 (m, 4H), 7.23- 7.13 (m, 2H), 7.05-6.95 (m, 2H), 3.78-3.70 (m, 6H), 3.44 (dd, J = 13.1, 6.4 Hz, 2H), 3.06-2.95 (m, 4H), 2.95-2.85 (m, 2H), 1.72- 1.48 (m, 2H), 1.49-1.27 (m, 2H), 0.95 (t, J = 7.4 Hz, 3H); MS m/z 557.30 [M + H]⁺. 52

UNC2076A + ¹H NMR (400 MHz, CDCl₃) δ 10.13 (s, 1H), 9.43 (d, J = 6.9 Hz, 1H), 8.54 (s, 1H), 8.25 (t, J = 5.4 Hz, 1H), 7.83 (d, J = 8.7 Hz, 2H), 7.69 (d, J = 8.7 Hz, 2H), 4.49-4.36 (m, 1H), 3.79-3.66 (m, 4H), 3.43 (dd, J = 12.9, 6.9 Hz, 2H), 3.06-2.94 (m, 4H), 2.15- 2.01 (m, 2H), 1.83-1.74 (m, 2H), 1.74-1.65 (m, 2H), 1.65-1.54 (m, 4H), 1.46- 1.32 (m, 2H), 0.92 (t, J = 13 Hz, 3H); MS m/z 503.30 [M + H]⁺. 53

UNC2077A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.15 (s, 1H), 9.37 (d, J = 4.1 Hz, 1H), 8.55 (s, 1H), 8.39 (t, J = 5.5 Hz, 1H), 7.81 (d, J = 8.8 Hz, 2H), 7.67 (d, J = 8.7 Hz, 2H), 3.77-3.66 (m, 4H), 3.48 (dd, J = 13.0, 6.9 Hz, 2H), 3.09-3.01 (m, 1H), 3.01-2.92 (m, 5H), 1.67- 1.56 (m, 2H), 1.43-1.31 (m, 2H), 0.95-0.89 (m, 4H), 0.76-0.62 (m, 2H); MS m/z 475.20 [M + H]⁺. 54

UNC2093A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.71-8.51 (m, 2H), 8.51-8.40 (m, 1H), 8.04-7.90 (m, 1H), 7.90- 7.74 (m, 2H), 7.74-7.61 (m, 2H), 7.60-7.50 (m, 1H), 4.90-4.77 (m, 2H), 3.78- 3.61 (m, 4H), 3.40-3.24 (m, 2H), 3.04-2.85 (m, 4H), 1.57-1.36 (m, 2H), 1.38- 1.16 (m, 2H), 0.93-0.75 (m, 3H); MS m/z 526.25 [M + H]⁺. 55

UNC2081A + ¹H NMR (400 MHz, CDCl₃) δ 10.31 (s, 1H), 8.25 (t, J = 4.8 Hz, 1H), 7.94 (s, 1H), 7.86 (d, J = 8.7 Hz, 2H), 7.70 (d, J = 8.7 Hz, 2H), 3.78 (s, 8H), 3.76-3.70 (m, 4H), 3.38 (dd, J = 12.7, 7.0 Hz, 2H), 3.05- 2.90 (m, 4H), 1.62-1.51 (m, 2H), 1.41-1.30 (m, 2H), 0.89 (t, J = 13 Hz, 3H); MS m/z 505.25 [M + H]⁺. 56

UNC2082A ++ ¹H NMR (400 MHz, CDCl₃) δ 9.98 (s, 1H), 9.42 (d, J = 7.6 Hz, 1H), 8.58 (s, 1H), 8.16 (t, J = 5.2 Hz, 1H), 7.84 (d, J = 8.7 Hz, 2H), 7.69 (d, J = 8.6 Hz, 2H), 4.12-4.01 (m, 1H), 3.78-3.69 (m, 4H), 3.45- 3.36 (m, 2H), 3.05-2.93 (m, 4H), 2.06-1.93 (m, 2H), 1.85-1.72 (m, 2H), 1.70- 1.53 (m, 3H), 1.50-1.25 (m, 7H), 0.93 (t, J = 7.3 Hz, 3H); MS m/z 517.30 [M + H]⁺. 57

UNC2083A + ¹H NMR (400 MHz, CDCl₃) δ 10.21 (s, 1H), 9.51 (t, J = 5.7 Hz, 1H), 8.54 (s, 1H), 8.23 (s, 1H), 7.84 (d, J = 8.7 Hz, 2H), 7.69 (d, J = 8.6 Hz, 2H), 3.78-3.66 (m, 4H), 3.46- 3.34 (m, 4H), 3.03-2.94 (m, 4H), 1.83-1.73 (m, 4H), 1.72-1.63 (m, 2H), 1.62- 1.55 (m, 2H), 1.41-1.33 (m, 2H), 1.30-1.14 (m, 3H), 1.08-0.95 (m, 2H), 0.92 (t, J = 7.3 Hz, 3H); MS m/z 531.30 [M + H]⁺. 58

UNC2089A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.57 (s, 1H), 7.91 (d, J = 8.7 Hz, 2H), 7.76 (dd, J = 6.2, 4.7 Hz, 2H), 3.75-3.64 (m, 5H), 3.56-3.50 (m, 2H), 3.48- 3.41 (m, 2H), 3.32-3.27 (m, 4H), 2.99-2.91 (m, 4H), 2.60-2.47 (m, 1H), 2.27- 2.15 (m, 1H), 1.72-1.61 (m, 2H), 1.51-1.37 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 504.30 [M + H]⁺. 59

UNC2090A ++ ¹H NMR (400 MHz, CDCl₃) δ 10.53 (s, 1H), 9.83 (t, J = 5.4 Hz, 1H), 9.32-9.18 (m, 1H), 8.74 (s, 1H), 7.63 (d, J = 8.5 Hz, 2H), 7.56 (d, J = 8.4 Hz, 2H), 3.71 (s, 4H), 3.62-3.50 (m, 3H), 3.37 (ddd, J = 30.0, 12.9, 5.7 Hz, 3H), 2.95 (s, 5H), 2.86-2.74 (m, 1H), 2.49-2.34 (m, 1H), 2.09-1.83 (m, 3H), 1.67- 1.53 (m, 2H), 1.48-1.24 (m, 3H), 0.93 (t, J = 7.3 Hz, 3H); MS m/z 532.30 [M + H]⁺. 60

UNC2091A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.56 (s, 1H), 7.94-7.87 (m, 2H), 7.79- 7.71 (m, 2H), 3.74-3.63 (m, 5H), 3.56-3.50 (m, 3H), 3.47-3.39 (m, 3H), 3.00- 2.90 (m, 4H), 2.59-2.46 (m, 1H), 2.27-2.15 (m, 1H), 1.72-1.61 (m, 2H), 1.53- 1.38 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 504.30 [M + H]⁺.

Example 3 2-(Butylamino)-N-(4-fluorobenzyl)-4-(((trans)-4-hydroxycyclohexyl)amino)pyrimidine-5-carboxamide General Procedure B:

Methyl 2-(butylamino)-4-(((trans)-4-hydroxycyclohexyl)amino)pyrimidine-5-carboxylate

To a solution of 2,4-dichloropyrimidine-5-carbonyl chloride (500 mg, 2.38 mmol) in dichloromethane (30 mL) was added methanol (87.6 mg, 2.73 mmol) and diisopropylethylamine (369 mg, 2.86 mmol) at 0° C. The resulting mixture was stirred for 1 h at 0° C. Then the solvent was removed. The residue (461 mg, 94%) was dissolved in IPA (20 mL) and followed by the addition of trans-4-aminocyclohexanol (301.6 mg, 2.62 mmol) then DIEA (461.4 mg, 3.57 mmol) dropwisely. The resulting mixture was stirred at 0° C. for 90 min. After which butylamine (208.8 mg, 2.86 mmol) was added, followed by DIEA (461.4 mg, 3.57 mmol). The resulting mixture was stirred at room temperature for 3 h. Water was then added. The resulting mixture was extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄), filtered and concentrated. The residue was purified on ISCO to provide methyl 2-(butylamino)-4-(((trans-4-hydroxycyclohexyl)amino)pyrimidine-5-carboxylate (682.6 mg, 89% over 3 steps). ¹H NMR (400 MHz, CDCl₃) δ 9.21 (s, 1H), 8.77 (s, 1H), 6.29 (s, 1H), 4.81-4.64 (m, 1H), 4.51 (s, 3H), 4.46-4.38 (m, 1H), 4.13-4.11 (m, 2H), 2.89-2.81 (m, 2H), 2.74 (d, J=9.7 Hz, 2H), 2.35-2.25 (m, 2H), 2.23-2.00 (m, 6H), 1.67 (t, J=7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 167.9, 162.5, 161.3, 160.3, 95.5, 69.7, 51.2, 48.3, 41.1, 33.8, 31.7, 30.3, 20.1, 13.8; MS m/z 323.20 [M+H]⁺.

2-(Butylamino)-N-(4-fluorobenzyl)-4-(((trans)-4-hydroxycyclohexyl)amino)pyrimidine-5-carboxamide

A mixture of methyl 2-(butylamino)-4-(((trans-4-hydroxycyclohexyl)amino) pyrimidine-5-carboxylate (682.6 mg, 2.12 mmol) and lithium hydroxide monohydrate (888.4 mg, 21.2 mmol) in a mixture of methanol and water (25 mL, 3:2, v/v) was heated at reflux for 2 h. Then the reaction mixture was cooled to room temperature and acidified by a 4.0N solution of HCl (4N) to PH 3. The resulting mixture was extracted with EtOAc (4×). The combined organic layers were dried (Na₂SO₄) and concentrated to provide 2-(butylamino)-4-(((1r,4r)-4-hydroxycyclohexyl)amino)pyrimidine-5-carboxylic acid (647.1 mg, 99%), which was used in the next step without further purifications. MS m/z 309.30 [M+H]⁺.

A solution of the acid (61 mg, 0.20 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU, 81.4 mg, 0.25 mmol, 1.3 eq) and N,N-diisopropylethylamine (DIEA, 77.5 mg, 0.60 mmol, 3.0 eq) in anhydrous DMF (3.0 mL) and was added 4-fluorobenzylamine (37.5 mg, 0.30 mmol, 1.5 eq) in DMF (1.0 mL) dropwisely at room temperature. The resulting mixture was stirred for overnight, then diluted with EtOAc (15 mL) and washed with water (3×). The organic layer was dried (Na₂SO₄) and concentrated. The residue was purified on HPLC to give the title compound (61.5 mg, 74%) as a yellow solid. ¹H NMR (400 MHz, CDCl₃) δ 9.57 (d, J=7.4 Hz, 1H), 8.77 (s, 1H), 8.13 (s, 1H), 7.40-7.31 (m, 1H), 7.29-7.22 (m, 3H), 7.00 (t, J=8.6 Hz, 2H), 4.44 (d, J=5.2 Hz, 2H), 4.00 (s, 1H), 3.77-3.62 (m, 1H), 3.40 (dd, J=13.0, 6.9 Hz, 2H), 2.15-2.09 (m, 2H), 2.04 (d, J=7.6 Hz, 2H), 1.66-1.54 (m, 2H), 1.49-1.33 (m, 6H), 0.94 (t, J=7.3 Hz, 3H); MS m/z 416.30 [M+H]⁺.

Table 3 describes compounds prepared following procedures described in Example 3 (General Procedure B), using appropriate reagents.

Mer Physical Data MS m/z Structure Compound_ID IC₅₀ (M + 1) or/and ¹H NMR  1

UNC1844A +++ ¹H NMR (400 MHz, CDCl₃) δ 7.94 (s, 1H), 3.87 (s, 6H), 3.47 (t, J = 5.9 Hz, 3H), 3.25-3.19 (m, 2H), 3.15 (t, J = 6.6 Hz, 2H), 1.96 (d, J = 10.9 Hz, 2H), 1.85 (d, J = 10.3 Hz, 2H), 1.53-1.39 (m, 6H), 1.30-1.17 (m, 6H), 0.80 (t, J = 7.3 Hz, 3H); MS m/z 380.30 [M + H]⁺.  2

UNC1845A +++ ¹H NMR (400 MHz, CDCl₃) δ 9.50 (d, J = 7.4 Hz, 1H), 9.38 (t, J = 5.4 Hz, 1H), 7.82 (s, 1H), 7.09 (s, 1H), 4.03- 3.91 (m, 1H), 3.73-3.64 (m, 1H), 3.50 (t, J = 5.5 Hz, 2H), 3.45-3.35 (m, 4H), 3.34 (s, 3H), 2.12-2.05 (m, 2H), 2.05-1.98 (m, 2H), 1.84- 1.77 (m, 2H), 1.63-1.55 (m, 2H), 1.45-1.31 (m, 6H), 0.91 (t, J = 7.4 Hz, 3H); MS m/z 380.30 [M + H]⁺.  3

UNC1846A +++ ¹H NMR (400 MHz, CDCl₃) δ 8.17 (s, 1H), 7.31 (d, J = 8.3Hz, 2H), 7.08 (d, J = 8.2 Hz, 2H), 3.64 (t, J = 7.0 Hz, 2H), 3.55-3.46 (m, 1H), 3.30 (t, J = 7.2 Hz, 2H), 3.25-3.18 (m, 1H), 2.69 (t, J = 7.0 Hz, 2H), 2.01-1.94 (m, 2H), 1.90-1.85 (m, 2H), 1.54- 1.44 (m, 2H), 1.33-1.22 (m, 6H), 0.82 (t, J = 7.3 Hz, 3H); MS m/z 428.30 [M + H]⁺.  4

UNC1849A ++++ ¹H NMR (400 MHz, CDCl₃) δ 8.40 (d, J = 6.0 Hz, 2H), 8.11 (s, 1H), 7.27 (s, 2H), 7.21 (d, J = 6.0 Hz, 2H), 4.44 (s, 2H), 3.94-3.83 (m, 1H), 3.55 (s, 4H), 2.09-1.98 (m, 2H), 1.96-1.88 (m, 2H), 1.55-1.45 (m, 2H), 1.39- 1.21 (m, 6H), 0.88 (t, J = 7.3 Hz, 3H); MS m/z 399.30 [M + H]⁺.  5

UNC1850A +++ ¹H NMR (400 MHz, CDCl₃) δ 9.62 (d, J = 7.3 Hz, 1H), 8.34 (s, 1H), 8.24 (s, 1H), 7.18-7.13 (m, 2H), 7.01- 6.95 (m, 2H), 6.82-6.68 (m, 1H), 4.55-4.36 (m, 1H), 4.07-3.93 (m, 1H), 3.81- 3.67 (m, 1H), 3.64-3.50 (m, 2H), 3.43 (dd, J = 13.5, 6.6 Hz, 2H), 2.85 (t, J = 7.4 Hz, 2H), 2.16-2.01 (m, 4H), 1.69-1.55 (m, 2H), 1.53- 1.34 (m, 6H), 0.95 (t, J = 7.4 Hz, 3H); MS m/z 430.30 [M + H]⁺.  6

UNC1839A +++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 9.49 (d, J = 7.5 Hz, 1H), 8.08 (s, 1H), 3.89-3.81 (m, 4H), 3.72- 3.66 (m, 3H), 3.56-3.50 (m, 1H), 3.42-3.35 (m, 1H), 3.32-3.22 (m, 6H), 3.03- 2.96 (m, 2H), 2.84 (s, 2H), 2.08-1.94 (m, 2H), 1.94- 1.85 (m, 4H), 1.54-1.46 (m, 2H), 1.36-1.20 (m, 6H), 0.83 (t, J = 7.3 Hz, 3H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 169.4, 163.7, 156.7, 146.9, 104.1, 72.6, 67.7, 59.0, 55.7, 45.0, 40.3, 36.9, 34.7, 33.4, 27.2, 23.8, 17.4; MS m/z 435.35 [M + H]⁺.  7

UNC1840A ++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.08 (s, 1H), 3.90-3.64 (m, 8H), 3.46-3.37 (m, 3H), 3.35- 3.21 (m, 5H), 3.04-2.94 (m, 2H), 2.83 (s, 1H), 1.97-1.86 (m, 2H), 1.57-1.45 (m, 4H), 1.36-1.23 (m, 4H), 0.84 (q, J = 7.3 Hz, 6H); ¹³C NMR (101 MHz, CD₃OD + CDCl₃) δ 161.4, 156.3, 148.7, 138.6, 96.1, 51.0, 47.9, 36.9, 36.5, 32.3, 26.5, 19.2, 15.9, 15.7, 9.4; MS m/z 393.30 [M + H]⁺.  8

UNC2579A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.80-8.74 (m, 1H), 8.49 (td, J = 7.9, 1.6 Hz, 1H), 8.40 (s, 1H), 8.00 (d, J = 8.1 Hz, 1H), 7.93- 7.87 (m, 1H), 4.84 (s, 2H), 4.11-3.99 (m, 1H), 3.68- 3.55 (m, 1H), 3.48 (t, J = 7.1 Hz, 2H), 2.19-1.90 (m, 4H), 1.73-1.57 (m, 2H), 1.51-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 399.30 [M + H]⁺.  9

UNC2580A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.88 (M, 1H), 8.78 (d, J = 5.7 Hz, 1H), 8.64-8.57 (m, 1H), 8.34 (s, 1H), 8.08-8.02 (m, 1H), 4.70 (s, 2H), 4.11-3.99 (m, 1H), 3.69-3.57 (m, 1H), 3.47 (t, J = 7.1 Hz, 2H), 2.21-1.91 (m, 4H), 1.71-1.57 (m, 2H), 1.52-1.33 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H) ; MS m/z 399.30 [M + H]⁺.  10

UNC2581A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.27 (s, 1H), 7.59-7.52 (m, 4H), 4.56- 4.50 (m, 2H), 4.13-3.99 (m, 1H), 3.68-3.56 (m, 1H), 3.46 (dd, J = 13.1, 6.2 Hz, 2H), 3.26 (s, 6H), 2.25-2.05 (m, 2H), 2.00 (d, J = 9.3 Hz, 2H), 1.73-1.55 (m, 2H), 1.45 (td, J = 14.8, 7.3 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 441.35 [M + H]⁺.  11

UNC2582A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.27 (s, 1H), 7.71 (d, J = 7.9 Hz, 1H), 7.65- 7.52 (m, 2H), 7.46 (t, J = 7.5 Hz, 1H), 4.70 (s, 2H), 4.17-3.96 (m, 1H), 3.72-3.50 (m, 2H), 3.45 (dd, J = 33.1, 26.3 Hz, 2H), 3.31 (dt, J = 3.3, 1.6 Hz, 4H), 2.11 (d, J = 11. 2 Hz, 2H), 2.00 (d, J = 10.6 Hz, 2H), 1.65 (dt, J = 14.8, 7.5 Hz, 2H), 1.56-1.15 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 466.30 [M + H]⁺.  12

UNC2583A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 7.64 (d, J = 8.1 Hz, 2H), 7.52 (d, J = 8.2 Hz, 2H), 4.57 (s, 2H), 4.11-4.00 (m, 1H), 3.71-3.57 (m, 1H), 3.51- 3.42 (m, 2H), 2.18-1.95 (m, 4H), 1.71-1.58 (m, 2H), 1.52-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 466.25 [M + H]⁺.  13

UNC2591A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.26 (s, 1H), 7.61-7.57 (m, 4H), 7.45- 7.39 (m, 4H), 7.35-7.29 (m, 1H), 4.53 (s, 2H), 4.10-4.00 (m, 1H), 3.70-3.58 (m, 2H), 3.52-3.40 (m, 2H), 2.17- 1.95 (m, 4H), 1.71-1.59 (m, 2H), 1.51-1.38 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 474.30 [M + H]⁺.  14

UNC2592A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 7.24 (t, J = 7.9 Hz, 1H), 6.93- 6.87 (m, 2H), 6.85-6.80 (m, 1H), 4.46 (s, 2H), 4.10-3.98 (m, 1H), 3.78 (s, 3H), 3.69- 3.57 (m, 1H), 3.47 (t, J = 6.9 Hz, 2H), 2.11 (d, J = 10.6 Hz, 2H), 2.00 (d, J = 10.2 Hz, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.52-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 428.30 [M + H]⁺.  15

UNC2584A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 6.48 (d, J = 2.3 Hz, 2H), 6.39 (t, J = 2.3 Hz, 1H), 4.42 (s, 2H), 4.10-3.99 (m, 2H), 3.76 (s, 6H), 3.70-3.56 (m, 2H), 3.52-3.42 (m, 2H), 2.17- 2.06 (m, 2H), 2.06-1.96 (m, 2H), 1.65 (dt, J = 15.1, 7.5 Hz, 2H), 1.54-1.36 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 458.30 [M + H]⁺.  16

UNC2585A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.16 (s, 1H), 7.17 (d, J = 8.3 Hz, 1H), 6.54 (d, J = 2.3 Hz, 1H), 6.48 (dd, J = 8.3, 2.4 Hz, 1H), 4.40 (s, 2H), 4.10-3.99 (m, 2H), 3.84 (s, 3H), 3.78 (s, 3H), 3.52- 3.42 (m, 2H), 2.16-2.07 (m, 2H), 2.04-1.96 (m, 2H), 1.64 (dt, J = 14.8, 7.6 Hz, 2H), 1.43 (dd, J = 15.0, 7.2 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 458.30 [M + H]⁺.  17

UNC2593A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.36 (s, 1H), 7.60 (s, 1H), 7.56-7.49 (m, 1H), 7.44 (t, J = 6.8 Hz, 2H), 4.55 (s, 2H), 4.10-4.01 (m, 1H), 3.75 (bs, 4H), 3.69-3.57 (m, 2H), 3.48 (t, J = 6.9 Hz, 2H), 2.33-2.24 (m, 4H), 2.17-2.05 (m, 2H), 2.05-1.94 (m, 2H), 1.65 (dt, J = 12.6, 7.6 Hz, 2H), 1.53-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 467.30 [M + H]⁺.  18

UNC2587A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.31 (s, 1H), 7.62 (d, J = 8.2 Hz, 2H), 7.49 (d, J = 8.2 Hz, 2H), 4.53 (s, 2H), 4.50 (s, 2H), 4.10-3.99 (m, 1H), 3.76-3.54 (m, 8H), 3.48 (t, J = 7.0 Hz, 2H), 3.01 (s, 3H), 2.16-2.06 (m, 2H), 2.04-1.96 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.51- 1.36 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 510.40 [M + H]⁺.  19

UNC2586A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 7.54 (d, J = 7.4 Hz, 1H), 7.43 (d, J = 8.1 Hz, 1H), 7.23 (dtd, J = 22.9, 7.3, 1.2 Hz, 2H), 6.72 (s, 1H), 4.65 (s, 2H), 4.12-4.00 (m, 2H), 3.68- 3.60 (m, 2H), 3.50-3.42 (m, 2H), 2.17-1.95 (m, 4H), 1.65 (dt, J = 14.9, 7.3 Hz, 2H), 1.53-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 438.30 [M + H]⁺.  20

UNC2594A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.65 (d, J = 2.7 Hz, 1H), 8.51 (d, J = 1.8 Hz, 1H), 8.37 (s, 1H), 8.23 (dd, J = 8.6, 2.2 Hz, 1H), 8.08 (d, J = 8.6 Hz, 1H), 7.89 (d, J = 1.6 Hz, 1H), 6.65 (dd, J = 2.6, 1.8 Hz, 1H), 4.59 (s, 2H), 4.10-4.00 (m, 1H), 3.67-3.57 (m, 2H), 3.47 (t, J = 6.9 Hz, 2H), 2.16-2.06 (m, 2H), 2.05-1.93 (m, 2H), 1.65 (dt, J = 12.6, 7.6 Hz, 2H), 1.52-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 465.30 [M + H]⁺.  21

UNC2595A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.47 (dd, J = 8.9, 2.2 Hz, 1H), 8.42 (s, 1H), 8.37 (d, J = 1.8 Hz, 1H), 7.48 (d, J = 8.9 Hz, 1H), 4.58 (s, 2H), 4.11-3.98 (m, 1H), 3.68-3.57 (m, 1H), 3.47 (t, J = 7.1 Hz, 2H), 2.63 (q, J = 7.5 Hz, 2H), 2.17-1.94 (m, 4H), 1.65 (dt, J = 12.6, 7.6 Hz, 2H), 1.50-1.34 (m, 6H), 1.24 (t, J = 7.5 Hz, 3H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 470.30 [M + H]⁺.  22

UNC2598A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.69 (d, J = 1.8 Hz, 1H), 8.48 (dd, J = 8.5, 2.1 Hz, 1H), 8.43 (s, 1H), 8.23 (d, J = 8.5 Hz, 1H), 8.04 (dd, J = 3.9, 1.1 Hz, 1H), 7.93 (dd, J = 5.0, 1.1 Hz, 1H), 7.35 (dd, J = 5.0, 3.9 Hz, 1H), 4.66 (s, 2H), 4.10-3.99 (m, 1H), 3.66- 3.57 (m, 1H), 3.48 (t, J = 7.0 Hz, 2H), 2.18-2.04 (m, 2H), 2.04-1.94 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.50-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 481.30 [M + H]⁺.  23

UNC2599A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.68 (d, J = 1.7 Hz, 1H), 8.53 (dd, J = 8.6, 2.0 Hz, 1H), 8.43 (s, 1H), 8.29 (d, J = 8.6 Hz, 1H), 7.99 (d, J = 1.7 Hz, 1H), 7.64 (d, J = 3.7 Hz, 1H), 6.83 (dd, J = 3.7, 1.8 Hz, 1H), 4.66 (s, 2H), 4.12-4.00 (m, 1H), 3.66-3.57 (m, 2H), 3.48 (t, J = 7.1 Hz, 2H), 2.16-2.04 (m, 2H), 2.04- 1.92 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.54-1.32 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 465.30 [M + H]⁺.  24

UNC2600A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.34 (s, 1H), 7.61-7.54 (m, 2H), 7.53- 7.47 (m, 3H), 4.34 (s, 2H), 4.14-3.98 (m, 2H), 3.69- 3.58 (m, 2H), 3.59-3.50 (m, 2H), 3.50-3.41 (m, 2H), 3.25-3.10 (m, 2H), 2.25- 2.05 (m, 4H), 2.05-1.92 (m, 3H), 1.64 (dt, J = 15.0, 7.5 Hz, 2H), 1.52-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 481.40 [M + H]⁺.  25

UNC2601A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.33 (s, 1H), 4.13-3.96 (m, 3H), 3.64- 3.50 (m, 4H), 3.50-3.37 (m, 3H), 3.13 (t, J = 11.9 Hz, 2H), 2.86 (s, 3H), 2.25-1.84 (m, 10H), 1.63 (dt, J = 14.9, 7.5 Hz, 2H), 1.49-1.33 (m, 6H), 0.97 (t, J = 7.4 Hz, 3H); MS m/z 405.30 [M + H]⁺.  26

UNC2602A ++++ ¹H MR (400 MHz, CD₃OD) δ 8.22 (s, 1H), 4.11-3.96 (m, 1H), 3.85- 3.71 (m, 1H), 3.69-3.59 (m, 1H), 3.52-3.42 (m, 2H), 2.17-2.05 (m, 2H), 2.05- 1.94 (m, 2H), 1.95-1.87 (m, 2H), 1.87-1.75 (m, 2H), 1.73-1.58 (m, 3H), 1.51- 1.14 (m, 12H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 390.30 [M + H]⁺.  27

UNC2603A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 4.10-3.97 (m, 1H), 3.70- 3.59 (m, 1H), 3.53-3.41 (m, 2H), 3.13 (d, J = 7.0 Hz, 2H), 2.16-1.94 (m, 4H), 1.82-1.71 (m, 4H), 1.71- 1.51 (m, 4H), 1.50-1.35 (m, 6H), 1.35-1.18 (m, 4H), 0.99 (dd, J = 9.7, 5.0 Hz, 5H); MS m/z 404.35 [M + H]⁺.  28

UNC2604A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.25 (s, 1H), 4.18 (s, 2H), 4.10-3.99 (m, 1H), 3.67-3.59 (m, 1H), 3.61- 3.53 (m, 2H), 3.53-3.43 (m, 4H), 2.17-1.95 (m, 4H), 1.75-1.60 (m, 6H), 1.60- 1.53 (m, 2H), 1.52-1.33 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 433.30 [M + H]⁺.  29

UNC2605A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 4.10-3.98 (m, 1H), 3.94 (dd, J = 11.5, 2.6 Hz, 2H), 3.69- 3.58 (m, 1H), 3.52-3.44 (m, 2H), 3.40 (td, J = 11.8, 2.1 Hz, 2H), 3.20 (d, J = 6.9 Hz, 2H), 2.17-1.96 (m, 4H), 1.90-1.77 (m, 1H), 1.71- 1.60 (m, 4H), 1.53-1.37 (m, 6H), 1.37-1.24 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 406.30 [M + H]⁺.  30

UNC2607A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.47 (s, 1H), 4.11-4.00 (m, 3H), 3.99- 3.86 (m, 2H), 3.75 (t, J = 5.8 Hz, 2H), 3.71-3.60 (m, 3H), 3.48 (t, J = 7.1 Hz, 2H), 3.40 (t, J = 5.8 Hz, 2H), 3.20 (td, J = 12.3, 3.8 Hz, 2H), 2.18-1.96 (m, 4H), 1.65 (dt, J = 12.6, 7.6 Hz, 2H), 1.55- 1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 421.30 [M + H]⁺.  31

UNC2627A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.42 (s, 1H), 7.30 (t, J = 2.2 Hz, 1H), 7.25 (t, J = 8.1 Hz, 1H), 7.18-7.13 (m, 1H), 6.74 (ddd, J = 8.2, 2.5, 0.8 Hz, 1H), 4.16-4.04 (m, 1H), 3.80 (s, 3H), 3.70-3.59 (m, 2H), 3.50 (t, J = 7.0 Hz, 2H), 2.20-2.07 (m, 2H), 2.07-1.96 (m, 2H), 1.67 (dt, J = 12.6, 7.6 Hz, 2H), 1.58- 1.34 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 414.30 [M + H]⁺.  32

UNC2628A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.51 (s, 1H), 7.89-7.83 (m, 2H), 7.63 (d, J = 9.1 Hz, 2H), 4.15-4.03 (m, 4H), 3.70-3.59 (m, 4H), 3.50 (t, J = 7.0 Hz, 2H), 2.19- 2.08 (m, 2H), 2.06-1.97 (m, 2H), 1.67 (dt, J = 12.7, 7.5 Hz, 2H), 1.56-1.35 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 469.30 [M + H]⁺.  33

UNC2629A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.52 (s, 1H), 7.83-7.77 (m, 2H), 7.57 (d, J = 8.6 Hz, 2H), 4.36 (s, 2H), 4.16-3.99 (m, 3H), 3.78 (dt, J = 19.6, 4.1 Hz, 2H), 3.67- 3.58 (m, 2H), 3.50 (t, J = 7.4 Hz, 2H), 3.42-3.34 (m, 3H), 3.21 (td, J = 12.4, 3.7 Hz, 2H), 2.19-2.08 (m, 2H), 2.07-1.94 (m, 2H), 1.67 (dt, J = 12.7, 7.6 Hz, 2H), 1.58- 1.33 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 483.35 [M + H]⁺.  34

UNC2694A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.61 (d, J = 5.3 Hz, 2H), 8.36 (s, 1H), 7.01 (t, J = 5.3 Hz, 1H), 4.58 (d, J = 13.4 Hz, 2H), 4.29-4.18 (m, 1H), 4.10-4.00 (m, 1H), 3.69- 3.60 (m, 1H), 3.51- 3.38 (m, 4H), 2.20-2.07 (m, 4H), 2.01 (d, J = 9.9 Hz, 2H), 1.84-1.70 (m, 2H), 1.70- 1.59 (m, 2H), 1.53- 1.33 (m, 6H), 1.15 (d, J = 6.2 Hz, 1H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 469.30 [M + H]⁺.  35

UNC2695A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.37 (s, 1H), 4.43 (tt, J = 12.3, 3.6 Hz, 1H), 4.11-3.99 (m, 1H), 3.98- 3.87 (m, 1H), 3.69-3.60 (m, 1H), 3.48 (t, J = 7.0 Hz, 2H), 2.85 (s, 3H), 2.23-2.06 (m, 4H), 1.98 (t, J = 13.1 Hz, 4H), 1.72-1.60 (m, 2H), 1.54 (d, J = 11.5 Hz, 12H), 1.49- 1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 461.40 [M + H]⁺.  36

UNC2696A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.37 (s, 1H), 4.19-4.01 (m, 3H), 3.97- 3.88 (m, 1H), 3.69-3.58 (m, 2H), 3.58-3.40 (m, 5H), 3.26-3.10 (m, 2H), 2.29- 2.16 (m, 2H), 2.16-1.93 (m, 7H), 1.72-1.58 (m, 2H), 1.51-1.34 (m, 12H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 433.40 [M + H]⁺.  37

UNC2697A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.46 (d, J = 17.7 Hz, 1H), 4.84-4.74 (m, 1H), 4.74-4.63 (m, 1H), 4.63- 4.55 (m, 2H), 4.35-4.22 (m, 2H), 4.13-4.00 (m, 1H), 3.70-3.59 (m, 1H), 3.54- 3.41 (m, 2H), 3.02 (d, J = 20.7 Hz, 3H), 2.17-2.06 (m, 2H), 2.06-1.96 (m, 2H), 1.71-1.59 (m, 2H), 1.53- 1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 377.30 [M + H]⁺  38

UNC2698A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.34 (s, 1H), 4.19-4.00 (m, 2H), 3.77- 3.55 (m, 6H), 3.55-3.41 (m, 2H), 3.30-3.11 (m, 4H), 2.91 (s, 3H), 2.58-2.43 (m, 2H), 2.30-2.16 (m, 4H), 2.15- 1.95 (m, 6H), 1.65 (dt, J = 14.9, 7.5 Hz, 2H), 1.53-1.36 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 488.40 [M + H]⁺.  39

UNC2732A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.25 (s, 1H), 4.09-3.92 (m, 4H), 3.70- 3.60 (m, 2H), 3.54-3.42 (m, 4H), 2.17-1.96 (m, 4H), 1.91-1.82 (m, 2H), 1.71- 1.57 (m, 5H), 1.50-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 492.30 [M + H]⁺.  40

UNC2733A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 4.28-4.15 (m, 1H), 4.09- 3.97 (m, 1H), 3.69-3.60 (m, 1H), 3.51-3.40 (m, 2H), 2.17-2.06 (m, 2H), 2.05- 1.94 (m, 4H), 1.81-1.70 (m, 2H), 1.68-1.57 (m, 4H), 1.57-1.48 (m, 2H), 1.48- 1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 476.30 [M + H]⁺.  41

UNC2734A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.18 (s, 1H), 4.09-3.90 (m, 3H), 3.69- 3.60 (m, 1H), 3.50-3.38 (m, 2H), 2.18-2.04 (m, 2H), 2.04-1.86 (m, 4H), 1.77- 1.50 (m, 13H), 1.50-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 404.30 [M + H]⁺.  42

UNC2735A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.34 (s, 1H), 7.56 (d, J = 8.2 Hz, 2H), 7.48 (d, J = 8.2 Hz, 2H), 4.53 (s, 2H), 4.36 (s, 2H), 4.10-3.98 (m, 3H), 3.84-3.75 (m, 2H), 3.68-3.57 (m, 2H), 3.48 (t, J = 6.9 Hz, 2H), 3.36 (d, J = 12.9 Hz, 2H), 3.20 (td, J = 12.4, 3.6 Hz, 2H), 2.19-2.06 (m, 2H), 2.04-1.94 (m, 2H), 1.65 (dt, J = 12.7, 7.5 Hz, 2H), 1.43 (dd, J = 18.5, 11.2 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 497.40 [M + H]⁺.  43

UNC2736A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.16 (s, 1H), 4.11-3.98 (m, 2H), 3.71- 3.60 (m, 2H), 3.50-3.41 (m, 2H), 2.82-2.72 (m, 1H), 2.17-2.06 (m, 2H), 2.06- 1.95 (m, 2H), 1.64 (dt, J = 14.9, 7.5 Hz, 2H), 1.43 (dq, J = 14.7, 7.3 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H), 0.84- 0.74 (m, 2H), 0.59 (td, J = 7.0, 5.0 Hz, 2H); MS m/z 448.30 [M + H]⁺.  44

UNC2737A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.25 (s, 1H), 4.47-4.34 (m, 1H), 4.09- 3.97 (m, 1H), 3.70-3.58 (m, 1H), 3.53-3.40 (m, 2H), 2.38-2.24 (m, 2H), 2.17- 1.95 (m, 7H), 1.84-1.72 (m, 2H), 1.69-1.59 (m, 2H), 1.52-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 362.30 [M + H]⁺.  45

UNC2742A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.32 (s, 1H), 4.10-3.99 (m, 1H), 3.68- 3.59 (m, 1H), 3.57-3.43 (m, 3H), 3.27 (d, J = 6.6 Hz, 2H), 3.05-2.93 (m, 2H), 2.85 (s, 3H), 2.16-1.93 (m, 6H), 1.71-1.60 (m, 2H), 1.60- 1.49 (m, 2H), 1.44 (dt, J = 15.1, 7.4 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 419.40 [M + H]⁺.  46

UNC2743A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.30 (s, 1H), 4.11-3.98 (m, 1H), 3.68- 3.59 (m, 3H), 3.55-3.42 (m, 3H), 3.27 (d, J = 6.5 Hz, 2H), 3.03-2.90 (m, 2H), 2.24-2.07 (m, 4H), 2.07- 1.93 (m, 5H), 1.90-1.79 (m, 2H), 1.79-1.59 (m, 7H), 1.59-1.51 (m, 2H), 1.48- 1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 473.40 [M + H]⁺.  47

UNC2744A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.25 (s, 1H), 8.20 (d, J = 2.5 Hz, 1H), 7.75- 7.69 (m, 3H), 7.47 (d, J = 8.6 Hz, 2H), 6.55-6.49 (m, 1H), 4.53 (s, 2H), 4.11-4.00 (m, 1H), 3.70-3.57 (m, 2H), 3.51-3.42 (m, 2H), 2.18- 2.05 (m, 2H), 2.05-1.95 (m, 2H), 1.71-1.59 (m, 2H), 1.52-1.35 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 464.30 [M + H]⁺.  48

UNC2761A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 7.43 (dd, J = 1.8, 0.8 Hz, 1H), 6.36 (dd, J = 3.2, 1.9 Hz, 1H), 6.30 (dd, J = 3.2, 0.6 Hz, 1H), 4.48 (s, 2H), 4.10- 4.00 (m, 1H), 3.69-3.59 (m, 1H), 3.46 (t, J = 6.8 Hz, 2H), 2.16-2.05 (m, 2H), 2.05- 1.96 (m, 2H), 1.64 (dt, J = 14.9, 7.5 Hz, 2H), 1.53-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 388.30 [M + H]⁺.  49

UNC2762A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.30 (dd, J = 5.1, 1.2 Hz, 1H), 7.04 (dd, J = 3.4, 1.0 Hz, 1H), 6.95 (dd, J = 5.1, 3.5 Hz, 1H), 4.65 (s, 2H), 4.11- 3.99 (m, 1H), 3.65 (td, J = 9.5, 4.2 Hz, 1H), 3.46 (t, J = 6.8 Hz, 2H), 2.19-2.06 (m, 2H), 2.06-1.95 (m, 2H), 1.64 (dt, J = 14.9, 7.5 Hz, 2H), 1.56-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H) ; MS m/z 404.20 [M + H]⁺.  50

UNC2763A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.17 (s, 1H), 8.09 (d, J = 8.1 Hz, 1H), 7.90 (d, J = 7.8 Hz, 1H), 7.83 (d, J = 8.1 Hz, 1H), 7.58-7.49 (m, 3H), 7.46 (dd, J = 15.2, 7.8 Hz, 1H), 4.97 (s, 2H), 4.11-4.00 (m, 1H), 3.70-3.60 (m, 1H), 3.51-3.41 (m, 2H), 2.17-2.07 (m, 2H), 2.07- 1.95 (m, 2H), 1.69-1.58 (m, 2H), 1.57-1.35 (m, 6H), 0.98 (t, J = 7.3 Hz, 3H); MS m/z 448.30 [M + H]⁺.  51

UNC2799A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.41 (s, 1H), 7.49 (d, J = 8.5 Hz, 2H), 7.17 (d, J = 8.5 Hz, 2H), 4.15-4.02 (m, 1H), 3.71-3.57 (m, 1H), 3.49 (t, J = 6.7 Hz, 2H), 2.66-2.55 (m, 2H), 2.18- 2.07 (m, 2H), 2.07-1.96 (m, 2H), 1.72-1.53 (m, 4H), 1.53-1.28 (m, 8H), 1.01 (t, J = 7.4 Hz, 3H), 0.94 (t, J = 7.4 Hz, 3H); MS m/z 440.30 [M + H]⁺.  52

UNC2764A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.81 (s, 1H), 8.10 (d, J = 8.3 Hz, 2H), 7.93 (d, J = 8.2 Hz, 2H), 4.80 (s, 2H), 4.44-4.34 (m, 1H), 4.14-3.85 (m, 8H), 3.79 (t, J = 7.1 Hz, 2H), 3.63-3.56 (m, 3H), 2.95 (s, 2H), 2.46-2.37 (m, 2H), 2.34-2.25 (m, 2H), 1.96 (dt, J = 15.0, 7.3 Hz, 2H), 1.84-1.65 (m, 6H), 1.29 (t, J = 7.3 Hz, 3H); MS m/z 496.40 [M + H]⁺.  53

UNC2775A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.37 (s, 1H), 7.74 (dd, J = 7.9, 1.4 Hz, 1H), 7.24-7.17 (m, 1H), 7.07 (dd, J = 8.3, 1.2 Hz, 1H), 6.96 (td, J = 7.7, 1.3 Hz, 1H), 4.14-4.02 (m, 1H), 3.89 (s, 3H), 3.69-3.60 (m, 1H), 3.50 (t, J = 7.4 Hz, 2H), 2.18- 2.05 (m, 2H), 2.05-1.94 (m, 2H), 1.72-1.62 (m, 2H), 1.55-1.32 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 414.30 [M + H]⁺.  54

UNC2776A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.38 (s, 1H), 7.53-7.45 (m, 2H), 6.96- 6.88 (m, 2H), 4.14-4.01 (m, 1H), 3.79 (s, 3H), 3.69-3.59 (m, 1H), 3.49 (t, J = 7.0 Hz, 2H), 2.17-2.07 (m, 2H), 2.06-1.97 (m, 2H), 1.67 (dt, J = 12.7, 7.6 Hz, 2H), 1.55- 1.35 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 414.30 [M + H]⁺.  55

UNC2800A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.36 (s, 1H), 7.39-7.24 (m, 5H), 4.20- 3.99 (m, 2H), 3.80-3.69 (m, 2H), 3.66-3.61 (m, 1H), 3.53-3.43 (m, 2H), 3.41- 3.33 (m, 2H), 3.22-3.15 (m, 1H), 3.15-3.07 (m, 3H), 2.30-2.17 (m, 2H), 2.15- 2.06 (m, 2H), 2.06-1.93 (m, 4H), 1.71-1.59 (m, 2H), 1.52-1.36 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 495.40 [M + H]⁺.  56

UNC2801A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.35 (s, 1H), 7.34-7.17 (m, 5H), 4.15- 3.98 (m, 2H), 3.70-3.59 (m, 3H), 3.53-3.42 (m, 3H), 3.18-3.04 (m, 4H), 2.73 (t, J = 7.4 Hz, 2H), 2.19 (d, J = 13.5 Hz, 2H), 2.15-2.04 (m, 5H), 2.04-1.88 (m, 4H), 1.65 (dt, J = 15.0, 7.6 Hz, 2H), 1.51-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 509.40 [M + H]⁺.  57

UNC2802A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.26 (s, 1H), 9.00 (d, J = 5.7 Hz, 1H), 8.94 (d, J = 7.9 Hz, 1H), 8.30 (s, 1H), 8.21 (dd, J = 8.1, 5.8 Hz, 1H), 4.66 (s, 2H), 4.09 (d, J = 36.9 Hz, 2H), 3.77- 3.53 (m, 4H), 3.53-3.41 (m, 2H), 2.29-2.14 (m, 3H), 2.14-1.93 (m, 6H), 1.73- 1.59 (m, 2H), 1.53-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 482.35 [M + H]⁺.  58

UNC2803A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.49 (s, 1H), 7.85 (d, J = 8.5 Hz, 2H), 7.65 (d, J = 8.7 Hz, 2H), 4.15-4.01 (m, 1H), 3.77-3.55 (m, 2H), 3.50 (t, J = 7.1 Hz, 2H), 2.21-2.08 (m, 2H), 2.08- 1.96 (m, 2H), 1.67 (dt, J = 14.9, 7.5 Hz, 2H), 1.56-1.33 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 452.25 [M + H]⁺.  59

UNC2804A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.33 (s, 1H), 7.70 (d, J = 8.7 Hz, 2H), 7.60 (d, J = 8.7 Hz, 2H), 4.55 (s, 2H), 4.11 (dd, J = 12.0, 7.0 Hz, 4H), 4.08-3.99 (m, 1H), 3.75-3.68 (m, 4H), 3.68- 3.58 (m, 1H), 3.48 (t, J = 7.0 Hz, 2H), 2.16-2.03 (m, 2H), 2.03-1.94 (m, 2H), 1.65 (dt, J = 14.9, 7.6 Hz, 2H), 1.51-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 483.30 [M + H]⁺.  60

UNC2805A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.50 (s, 1H), 7.64 (d, J = 8.5 Hz, 2H), 7.33 (d, J = 8.5 Hz, 2H), 4.07 (dd, J = 13.0, 3.4 Hz, 3H), 3.93- 3.83 (m, 2H), 3.70-3.62 (m, 1H), 3.58 (d, J = 13.0 Hz, 2H), 3.49 (t, J = 7.0 Hz, 2H), 3.45-3.36 (m, 2H), 3.22 (td, J = 12.3, 3.6 Hz, 2H), 3.17- 3.06 (m, 2H), 2.19-2.07 (m, 2H), 2.07-1.96 (m, 2H), 1.67 (dt, J = 12.7, 7.6 Hz, 2H), 1.55-1.35 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 497.35 [M + H]⁺.  61

UNC2806A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.47 (s, 1H), 7.64 (d, J = 8.5 Hz, 2H), 7.35 (d, J = 8.5 Hz, 2H), 4.15-4.04 (m, 2H), 4.03-3.72 (m, 5H), 3.72-3.58 (m, 4H), 3.58- 3.47 (m, 4H), 3.22-3.12 (m, 2H), 3.05 (s, 3H), 2.17-2.07 (m, 2H), 2.06-1.95 (m, 2H), 1.67 (dt, J = 14.9, 7.6 Hz, 2H), 1.56-1.35 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS mlz 510.40 [M + H]⁺.  62

UNC2876A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.38 (s, 1H), 4.15-3.98 (m, 2H), 3.79- 3.70 (m, 2H), 3.70-3.57 (m, 2H), 3.50 (dt, J = 14.5, 6.5 Hz, 2H), 3.19-3.08 (m, 2H), 3.05 (d, J = 7.3 Hz, 2H), 2.27-2.17 (m, 2H), 2.17- 2.03 (m, 3H), 2.03-1.93 (m, 3H), 1.71-1.59 (m, 2H), 1.52-1.37 (m, 6H), 1.21- 1.11 (m, 1H), 0.99 (t, J = 7.4 Hz, 3H), 0.82-0.74 (m, 2H), 0.52-0.43 (m, 2H); MS m/z 445.35 [M + H]⁺.  63

UNC2877A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.38 (s, 1H), 4.27-4.19 (m, 1H), 4.17- 3.99 (m, 2H), 3.69-3.58 (m, 3H), 3.55-3.40 (m, 3H), 3.16-3.04 (m, 2H), 2.98 (d, J = 6.6 Hz, 2H), 2.25-1.95 (m, 8H), 1.92-1.76 (m, 5H), 1.72 (d, J = 13.2 Hz, 1H), 1.69- 1.59 (m, 2H), 1.53-1.20 (m, 9H), 1.15-1.02 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 487.40 [M + H]⁺.  64

UNC2878A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.38 (s, 1H), 4.27-4.21 (m, 1H), 4.16- 3.99 (m, 2H), 3.75-3.60 (m, 3H), 3.55-3.43 (m, 3H), 3.25 (d, J = 7.2 Hz, 1H), 3.17- 3.05 (m, 3H), 2.40-2.28 (m, 1H), 2.25-1.90 (m, 10H), 1.80-1.59 (m, 6H), 1.53- 1.38 (m, 6H), 1.38-1.26 (m, 2H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 473.40 [M + H]⁺.  65

UNC2879A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.36 (s, 1H), 4.27-4.20 (m, 1H), 4.17- 3.99 (m, 2H), 3.77-3.59 (m, 3H), 3.59-3.41 (m, 4H), 3.18-3.05 (m, 2H), 2.28- 2.06 (m, 6H), 2.05-1.91 (m, 4H), 1.90-1.59 (m, 8H), 1.52-1.34 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 459.40 [M + H]⁺.  66

UNC2880A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 7.48-7.39 (m, 4H), 7.17- 7.14 (m, 2H), 6.29-6.24 (m, 2H), 4.50 (s, 2H), 4.10-3.99 (m, 1H), 3.71-3.54 (m, 2H), 3.52-3.40 (m, 2H), 2.16- 2.06 (m, 2H), 2.05-1.96 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.54-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 463.30 [M + H]⁺.  67

UNC2881A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.47 (t, J = 1.5 Hz, 1H), 8.35 (s, 1H), 8.08- 8.04 (m, 1H), 7.80-7.76 (m, 1H), 7.75-7.69 (m, 2H), 7.64 (d, J = 8.7 Hz, 2H), 4.59 (s, 2H), 4.11-3.97 (m, 1H), 3.69-3.57 (m, 2H), 3.48 (t, J = 7.0 Hz, 2H), 2.17-2.05 (m, 2H), 2.05-1.92 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.53-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 464.30 [M + H]⁺.  68

UNC2886A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.31 (s, 1H), 7.54 (s, 4H), 4.52 (s, 2H), 4.10- 4.00 (m, 1H), 3.80-3.68 (m, 4H), 3.68-3.59 (m, 2H), 3.47 (t, J = 6.8 Hz, 2H), 2.33- 2.22 (m, 4H), 2.16-2.06 (m, 2H), 2.05-1.94 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.51-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 467.40 [M + H]⁺.  69

UNC2918A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.34 (s, 1H), 7.66 (d, J = 8.7 Hz, 2H), 7.50 (d, J = 8.6 Hz, 2H), 4.34 (s, 2H), 4.16-4.03 (m, 2H), 4.03-3.96 (m, 4H), 3.70- 3.59 (m, 1H), 3.59-3.43 (m, 8H), 3.15 (t, J = 11.8 Hz, 2H), 2.19 (d, J = 13.9 Hz, 2H), 2.10 (d, J = 9.1 Hz, 2H), 2.05-1.90 (m, 4H), 1.70-1.59 (m, 2H), 1.43 (dd, J = 15.0, 7.3 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 566.40 [M + H]⁺.  70

UNC2956A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.33 (d, J = 1.6 Hz, 1H), 8.34 (s, 1H), 7.78 (s, 1H), 7.67 (d, J = 8.5 Hz, 2H), 7.62 (d, J = 8.6 Hz, 2H), 4.58 (s, 1H), 4.10-4.01 (m, 1H), 3.69-3.56 (m, 3H), 3.52-3.43 (m, 2H), 2.44 (s, 3H), 2.17-2.04 (m, 2H), 2.04-1.96 (m, 2H), 1.71- 1.59 (m, 2H), 1.51-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 478.30 [M + H]⁺.  71

UNC2969A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.32-8.24 (m, 1H), 7.81 (d, J = 7.8 Hz, 2H), 7.72 (d, J = 8.5 Hz, 2H), 7.60 (d, J = 8.4 Hz, 2H), 7.50 (t, J = 7.5 Hz, 2H), 7.45-7.38 (m, 1H), 4.59 (s, 2H), 4.11-3.97 (m, 2H), 3.70-3.56 (m, 2H), 3.54- 3.43 (m, 2H), 2.19-2.06 (m, 2H), 2.02-1.92 (m, 2H), 1.70-1.59 (m, 2H), 1.52- 1.36 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 540.30 [M + H]⁺.  72

UNC2957A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.32 (s, 1H), 7.88-7.85 (m, 1H), 7.84 (d, J = 2.1 Hz, 1H), 7.63-7.57 (m, 1H), 7.53 (d, J = 8.3 Hz, 2H), 7.50-7.46 (m, 4H), 7.44 (d, J = 8.4 Hz, 2H), 4.57 (s, 2H), 4.12-4.00 (m, 1H), 3.66-3.56 (m, 2H), 3.48 (t, J = 6.8 Hz, 2H), 2.17-1.93 (m, 4H), 1.72-1.59 (m, 2H), 1.43 (dd, J = 18.4, 10.8 Hz, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 540.30 [M + H]⁺.  73

UNC3004A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.36-8.31 (m, 1H), 7.64 (dd, J = 5.3, 3.1 Hz, 3H), 7.59 (d, J = 2.1 Hz, 1H), 7.54 (d, J = 8.5 Hz, 2H), 4.60 (s, 2H), 4.09-4.01 (m, 1H), 3.68-3.57 (m, 1H), 3.52-3.42 (m, 2H), 2.57 (s, 3H), 2.16-2.06 (m, 2H), 2.04-1.95 (m, 2H), 1.71- 1.60 (m, 2H), 1.50-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 478.30 [M + H]⁺.  74

UNC3111A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.43 (s, 1H), 7.15-7.09 (m, 2H), 7.03 (dd, J = 8.0, 1.9 Hz, 1H), 4.13- 3.99 (m, 1H), 3.68-3.58 (m, 1H), 3.50 (t, J = 6.8 Hz, 2H), 2.31 (s, 3H), 2.22 (s, 3H), 2.16-2.06 (m, 2H), 2.04- 1.94 (m, 2H), 1.73-1.60 (m, 2H), 1.54-1.34 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 412.30 [M + H]⁺.  75

UNC3112A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.35 (s, 1H), 7.50 (d, J = 2.6 Hz, 1H), 6.98 (d, J = 9.0 Hz, 1H), 6.75 (dd, J = 9.0, 3.0 Hz, 1H), 4.15- 4.01 (m, 1H), 3.85 (s, 3H), 3.76 (s, 3H), 3.69-3.57 (m, 2H), 3.50 (t, J = 6.9 Hz, 2H), 2.17-2.06 (m, 2H), 2.05- 1.97 (m, 2H), 1.67 (dt, J = 12.6, 7.6 Hz, 2H), 1.56-1.34 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H); MS m/z 444.30 [M + H]⁺.  76

UNC3144A ¹H NMR (400 MHz, CD₃OD) δ 9.05 (s, 1H), 8.30 (s, 1H), 7.61 (t, J = 1.7 Hz, 1H), 7.59-7.55 (m, 1H), 7.48-7.32 (m, 4H), 5.45 (s, 2H), 4.50 (s, 2H), 4.10-4.00 (m, 1H), 3.66-3.58 (m, 2H), 3.47 (t, J = 7.0 Hz, 2H), 2.17-2.05 (m, 2H), 2.04- 1.94 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.52-1.33 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 478.30 [M + H]⁺.  77

UNC3145A ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 0.9 Hz, 1H), 8.38-8.35 (m, 1H), 8.33 (s, 1H), 7.68-7.62 (m, 2H), 7.58 (d, J = 8.7 Hz, 2H), 4.57 (s, 2H), 4.12-3.99 (m, 1H), 3.68-3.60 (m, 2H), 3.48 (t, J = 6.9 Hz, 2H), 2.17-2.06 (m, 2H), 2.04- 1.95 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.53-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 533.30 [M + H]⁺.  78

UNC3183A ¹H NMR (400 MHz, CD₃OD) δ 9.36 (d, J = 1.5 Hz, 1H), 8.34 (s, 1H), 7.93 (s, 1H), 7.72-7.66 (m, 2H), 7.62 (d, J = 8.6 Hz, 2H), 4.73 (d, J = 0.6 Hz, 2H), 4.59 (s, 2H), 4.11-4.00 (m, 1H), 3.70-3.57 (m, 1H), 3.48 (t, J = 7.0 Hz, 2H), 2.17-2.05 (m, 2H), 2.05-1.93 (m, 2H), 1.65 (dt, J = 12.7, 7.6 Hz, 2H), 1.51-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 494.30 [M + H]⁺.  79

UNC4332A ¹H NMR (400 MHz, CD₃OD) δ 8.34 (d, J = 2.4 Hz, 1H), 8.22 (s, 1H), 7.80 (dd, J = 8.2, 2.4 Hz, 1H), 7.41 (d, J = 8.2 Hz, 1H), 4.48 (s, 2H), 4.06-3.97 (m, 1H), 3.65-3.55 (m, 1H), 3.45 (t, J = 6.5 Hz, 2H), 2.14-1.92 (m, 4H), 1.62 (qunit, J = 7.1 Hz, 2H), 1.50-1.30 (m, 6H), 0.97 (t, J = 7.2 Hz, 3H); MS m/z 433.0 [M + H]⁺.  80

UNC4234A ¹H NMR (400 MHz, CD₃OD) δ 8.81 (d, J = 1.7 Hz, 1H), 8.59 (dd, J = 8.4, 1.8 Hz, 1H), 8.42 (s, 1H), 8.29 (d, J = 8.4 Hz, 1H), 7.95-7.90 (m, 2H), 7.70- 7.62 (m, 3H), 4.70 (s, 2H), 4.07-3.97 (m, 1H), 3.67- 3.53 (m, 1H), 3.46 (t, J = 7.0 Hz, 2H), 2.12-1.92 (m, 4H), 1.63 (quint, J = 7.1 Hz, 2H), 1.50-1.30 (m, 6H), 0.97 (t, J = 7.3 Hz, 3H); MS m/z 475.0 [M + H]⁺.  81

UNC4235A ¹H NMR (400 MHz, CD₃OD) δ 8.86 (d, J = 1.6 Hz, 1H), 8.67 (dd, J = 8.5, 1.9 Hz, 1H), 8.53 (d, J = 1.5 Hz, 1H), 8.47 (d, J = 8.5 Hz, 1H), 8.44 (s, 1H), 8.15 (d, J = 8.7 Hz, 1H), 8.08 (d, J = 7.3 Hz, 1H), 8.00 (d, J = 7.4 Hz, 1H), 7.97 (dd, J = 8.6, 1.9 Hz, 1H), 7.72-7.62 (m, 2H), 4.73 (s, 2H), 4.10-3.97 (m, 1H), 3.64-3.54 (m, 1H), 3.46 (t, J = 7.0 Hz, 2H), 2.14-1.92 (m, 4H), 1.63 (quint, J = 7.2 Hz, 2H), 1.50-1.30 (m, 6H), 0.97 (t, J = 7.4 Hz, 3H); MS m/z 525.0 [M + H]⁺.  82

UNC4236A ¹H NMR (400 MHz, CD₃OD) δ 9.52 (d, J = 1.5 Hz, 1H), 9.25 (dt, J = 8.3, 1.6 Hz, 1H), 8.89 (d, J = 5.8 Hz, 1H), 8.79 (d, J = 1.8 Hz, 1H), 8.33 (s, 1H), 8.19 (dd, J = 8.3, 5.8 Hz, 1H), 8.16 (d, J = 8.2 Hz, 1H), 8.06 (d, J = 8.2 Hz, 1H), 4.60 (s, 2H), 4.08-3.97 (m, 1H), 3.65- 3.55 (m, 1H), 3.45 (t, J = 7.0 Hz, 2H), 2.14-1.92 (m, 4H), 1.63 (quint, J = 7.2 Hz, 2H), 1.51-1.31 (m, 6H), 0.97 (t, J = 7.4 Hz, 3H); MS m/z 476.0 [M + H]⁺.  83

UNC4238A ¹H NMR (400 MHz, CD₃OD) δ 8.70 (d, J = 1.4 Hz, 1H), 8.49 (dd, J = 8.6, 1.9 Hz, 1H), 8.38 (s, 1H), 8.23 (d, J = 8.5 Hz, 1H), 7.94-7.84 (m, 2H), 7.21- 7.15 (m, 2H), 4.65 (s, 2H), 4.11-3.97 (m, 1H), 3.90 (s, 3H), 3.66-3.54 (m, 1H), 3.45 (t, J = 7.0 Hz, 2H), 2.15-1.90 (m, 4H), 1.63 (quint, J = 7.4 Hz, 2H), 1.50-1.30 (m, 6H), 0.97 (t, J = 7.3 Hz, 3H); MS m/z 505.0 [M + H]⁺.  84

UNC4239A ¹H NMR (400 MHz, CD₃OD) δ 8.80 (d, J = 1.8 Hz, 1H), 8.33 (s, 1H), 8.31 (d, 1.8 Hz, 1H), 8.16 (d, J = 8.3 Hz, 1H), 8.12 (d, J = 8.3 Hz, 2H), 7.93 (d, J = 8.2 Hz, 2H), 4.65 (s, 2H), 4.08-3.98 (m, 1H), 3.66-3.54 (m, 1H), 3.45 (t, J = 7.0 Hz, 2H), 2.15-1.92 (m, 4H), 1.63 (quint, J = 7.6 Hz, 2H), 1.50-1.30 (m, 6H), 0.97 (t, J = 7.4 Hz, 3H); MS m/z 500.0 [M + H]⁺.  85

UNC4246A ¹H NMR (400 MHz, CD₃OD) δ 8.80 (d, J = 1.7 Hz, 1H), 8.54 (dd, J = 8.5, 2.0 Hz, 1H), 8.40 (s, 1H), 8.28 (d, J = 8.4 Hz, 1H), 7.60-7.54 (m, 1H), 7.52- 7.47 (m, 2H), 7.26-7.22 (m, 1H), 4.70 (s, 2H), 4.11-4.01 (m, 1H), 3.92 (s, 3H), 3.70- 3.55 (m, 1H), 3.48 (t, J = 7.0 Hz, 2H), 2.15-1.92 (m, 4H), 1.65 (quint, J = 7.6 Hz, 2H), 1.52-1.35 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 505.0 [M + H]⁺.  86

UNC4254A ¹H NMR (400 MHz, CD₃OD) δ 9.40 (s, 2H), 9.38 (s, 1H), 8.93 (d, J = 1.6 Hz, 1H), 8.75 (s, 1H), 8.50 (dd, J = 8.3, 1.9 Hz, 1H), 8.32 (d, J = 8.3 Hz, 1H), 4.70 (s, 2H), 4.10-3.98 (m, 1H), 3.66- 3.54 (m, 1H), 3.46 (t, J = 7.0 Hz, 2H), 2.15-1.90 (m, 4H), 1.63 (quint, J = 7.6 Hz, 2H), 1.50-1.30 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 477.0 [M + H]⁺.  87

UNC4255A ¹H NMR (400 MHz, CD₃OD) δ 8.78 (d, J = 1.8 Hz, 1H), 8.54 (dd, J = 8.5, 2.1 Hz, 1H), 8.40 (s, 1H), 8.19 (d, J = 8.4 Hz, 1H), 7.68-7.60 (m, 2H), 7.27 (d, J = 8.3 Hz, 1H), 7.19 (td, J = 7.6, 0.8 Hz, 1H), 4.68 (s, 2H), 4.08-3.98 (m, 1H), 3.93 (s, 3H), 3.67-3.54 (m, 1H), 3.46 (t, J = 7.1 Hz, 2H), 2.12-1.92 (m, 4H), 1.63 (quint, J = 7.1 Hz, 2H), 1.50-1.32 (m, 6H), 0.97 (t, J = 7.4 Hz, 3H); MS m/z 505.0 [M + H]⁺.  88

UNC4256A ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J = 1.7 Hz, 1H), 8.50 (dd, J = 8.6, 2.0 Hz, 1H), 8.38 (s, 1H), 8.07 (d, J = 8.6 Hz, 1H), 6.90 (s, 1H), 4.63 (s, 2H), 4.07-3.97 (m, 1H), 3.67- 3.55 (m, 1H), 3.45 (t, J = 7.0 Hz, 2H), 2.55-2.35 (m, 4H), 2.13-1.92 (m, 4H), 1.90- 1.83 (m, 2H), 1.76-1.70 (m, 2H), 1.63 (quint, J = 7.1 Hz, 2H), 1.50-1.30 (m, 6H), 0.97 (t, J = 7.3 Hz, 3H); MS m/z 479.0 [M + H]⁺.  89

UNC4260A ¹H NMR (400 MHz, CD₃OD) δ 8.92 (d, J = 1.3 Hz, 1H), 8.60 (d, J = 8.3 Hz, 1H), 8.45 (s, 1H), 8.03 (d, J = 8.2 Hz, 1H), 4.72 (s, 2H), 4.12-4.00 (m, 1H), 3.67- 3.57 (m, 1H), 3.48 (t, J = 7.1 Hz, 2H), 2.55 (s, 3H), 2.36 (s, 3H), 2.15-1.95 (m, 4H), 1.64 (quint, J = 7.0 Hz, 2H), 1.50-1.35 (m, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 494.0 [M + H]⁺.  90

UNC4247A ¹H NMR (400 MHz, CD₃OD) δ 8.32 (s, 1H), 7.88 (d, J = 3.4 Hz, 1H), 7.71 (d, J = 3.4 Hz, 1H), 4.87 (s, 2H), 4.10-4.00 (m, 1H), 3.67-3.57 (m, 1H), 3.48 (t, J = 7.1 Hz, 2H), 2.15-1.95 (m, 4H), 1.65 (quint, J = 7.0 Hz, 2H), 1.50-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 405.0 [M + H]⁺.  91

UNC4286A ¹H NMR (400 MHz, CD₃OD) δ 8.95 (d, J = 8.6 Hz, 1H), 8.49 (s, 1H), 8.26- 8.22 (m, 2H), 8.13-8.07 (m, 1H), 7.97 (d, J = 8.6 Hz, 1H), 7.93-7.87 (m, 1H), 4.98 (s, 2H), 4.08-3.98 (m, 1H), 3.67-3.57 (m, 1H), 3.48 (t, J = 7.1 Hz, 2H), 2.11-1.91 (m, 4H), 1.65 (quint, J = 7.0 Hz, 2H), 1.50-1.30 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 449.0 [M + H]⁺.  92

UNC4285A ¹H NMR (400 MHz, CD₃OD) δ 8.31 (s, 1H), 8.00 (d, J = 2.5 Hz, 1H), 6.60 (d, J = 2.5 Hz, 1H), 4.62 (s, 2H), 4.10-4.00 (m, 1H), 3.67-3.55 (m, 1H), 3.47 (t, J = 7.0 Hz, 2H), 2.15-1.95 (m, 4H), 1.64 (quint, J = 7.1 Hz, 2H), 1.50-1.34 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 388.0 [M + H]⁺.  93

UNC4287A ¹H NMR (400 MHz, CD₃OD) δ 8.29 (s, 1H), 4.10-4.00 (m, 1H), 3.68- 3.55 (m, 1H), 3.50-3.37 (m, 4H), 3.28-3.24 (m, 2H), 3.02-2.92 (m, 2H), 2.15- 1.90 (m, 7H), 1.64 (quint, J = 7.1 Hz, 2H), 1.53-1.33 (m, 8H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 405.0 [M + H]⁺.  94

UNC4288A ¹H NMR (400 MHz, CD₃OD) δ 8.20 (s, 1H), 4.55-4.46 (m, 1H), 4.09- 4.00 (m, 1H), 3.97-3.89 (m, 1H), 3.67-3.58 (m, 1H), 3.51-3.42 (m, 2H), 3.25- 3.18 (m, 2H), 3.14-3.05 (m, 1H), 2.66-2.57 (m, 1H), 2.16-1.94 (m, 7H), 1.87- 1.73 (m, 3H), 1.65 (quint, J = 7.1 Hz, 2H), 1.52-1.35 (m, 6H), 1.30-1.05 (m, 2H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 447.0 [M + H]⁺.  95

UNC4289A ¹H NMR (400 MHz, CD₃OD) δ 8.32 (s, 1H), 4.10-3.99 (m, 1H), 3.70- 3.55 (m, 2H), 3.53-3.43 (m, 4H), 3.30-3.24 (m, 2H), 3.07-2.96 (m, 2H), 2.20- 1.90 (m, 7H), 1.70-1.52 (m, 4H), 1.48-1.38 (m, 6H), 1.36 (d, J = 6.7 Hz, 6H), 0.99 (t, J = 7.3 Hz, 3H); MS m/z 447.0 [M + H]⁺.  96

UNC4290A ¹H NMR (400 MHz, CD₃OD) δ 8.61 (d, J = 1.6 Hz, 1H), 8.23 (s, 1H), 6.49 (d, J = 1.6 Hz, 1H), 4.59 (s, 2H), 4.10-4.00 (m, 1H), 3.67-3.55 (m, 1H), 3.47 (t, J = 7.0 Hz, 2H), 2.15-1.95 (m, 4H), 1.64 (quint, J = 7.1 Hz, 2H), 1.55-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 389.0 [M + H]⁺.  97

UNC4302A ¹H NMR (400 MHz, CD₃OD) δ 8.31 (s, 1H), 4.10-4.00 (m, 1H), 3.75- 3.40 (m, 6H), 3.30-3.24 (m, 2H), 3.20-3.10 (m, 1H), 3.09-2.97 (m, 1H), 2.15- 1.87 (m, 11H), 1.75-1.30 (m, 15H), 1.29-1.15 (m, 1H), 0.98 (t, J = 7.2 Hz, 3H); MS m/z 487.0 [M + H]⁺.  98

UNC4303A ¹H NMR (400 MHz, CD₃OD) δ 8.28 (s, 1H), 6.03-5.91 (m, 1H), 5.62- 5.56 (m, 2H), 4.10-4.00 (m, 1H), 3.76-3.71 (m, 2H), 3.68-3.54 (m, 3H), 3.50- 3.40 (m, 2H), 3.28-3.24 (m, 2H), 2.98-2.88 (m, 2H), 2.15- 1.85 (m, 7H), 1.64 (quint, J = 7.1 Hz, 2H), 1.54-1.35 (m, 8H), 0.99 (t, J = 7.2 Hz, 3H); MS m/z 445.0 [M + H]⁺.  99

UNC4304A ¹H NMR (400 MHz, CD₃OD) δ 8.33 (s, 1H), 7.70-7.49 (m, 5H), 4.10- 4.00 (m, 1H), 3.75-3.55 (m, 5H), 3.52-3.44 (m, 2H), 3.40-3.34 (m, 2H), 2.18- 1.96 (m, 7H), 1.91-1.78 (m, 2H), 1.65 (quint, J = 7.1 Hz, 2H), 1.52-1.34 (m, 6H), 0.99 (t, J = 7.1 Hz, 3H); MS m/z 481.0 [M + H]⁺. 100

UNC4307A ¹H NMR (400 MHz, CD₃OD) δ 9.14 (s, 1H), 8.89 (s, 2H), 8.29 (s, 1H), 4.55 (s, 2H), 4.10-4.00 (m, 1H), 3.67-3.57 (m, 1H), 3.46 (t, J = 7.0 Hz, 2H), 2.15-1.95 (m, 4H), 1.64 (quint, J = 7.1 Hz, 2H), 1.53-1.35 (m, 6H), 0.98 (t, J = 7.3 Hz, 3H); MS m/z 400.0 [M + H]⁺. 101

UNC4344A ¹H NMR (400 MHz, CD₃OD) δ 9.12 (s, 1H), 8.22 (s, 1H), 7.93 (s, 1H), 4.72 (s, 2H), 4.10-4.00 (m, 1H), 3.68-3.60 (m, 1H), 3.46 (t, J = 7.0 Hz, 2H), 2.15-1.95 (m, 4H), 1.64 (quint, J = 7.1 Hz, 2H), 1.55-1.32 (m, 6H), 0.98 (t, J = 7.3 Hz, 3H); MS m/z 405.0 [M + H]⁺.

Example 4 (1r,4r)-4-((2-(Butylamino)-5-(5-(morpholinosulfonyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol General Procedure C:

4-((6-Chloropyridin-3-yl)sulfonyl)morpholine

A solution of 2-chloropyridine-5-sulfonyl chloride (212 mg, 1.0 mmol) in DCM (10 mL) was added morpholine (87.1 mg, 1.0 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 10 min and then DIEA (194 mg, 1.5 mmol) was added dropwisely. The mixture was stirred at 0° C. for 2 h. Then the mixture was diluted with EtOAc (15 mL) and washed with water (2×). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was purified on ISCO to give the title compound as a white solid (246.1 mg, 94%). ¹H NMR (400 MHz, CDCl₃) δ 8.73-8.65 (m, 1H), 7.94 (dd, J=8.3, 2.5 Hz, 1H), 7.49 (dd, J=8.3, 0.6 Hz, 1H), 3.74-3.63 (m, 4H), 2.99 (dd, J=5.6, 3.9 Hz, 4H); ¹³C NMR (101 MHz, cdcl3) δ 155.9, 148.7, 137.9, 131.1, 124.9, 65.9, 45.8; MS m/z 263.30 [M+H]⁺.

(1r,4r)-4-((2-(Butylamino)-5-(5-(morpholinosulfonyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol

A 10 mL microwave tube was charged with 2,4-dichloropyrimidine-5-boronic acid pinacol ester (55 mg, 0.20 mmol), K₂CO₃ (41.5 mg, 0.30 mmol) and THF (2.0 mL) The resulting mixture was then heated to 80° C. for 15 min under Microwave irradiation. Then 4-((6-chloropyridin-3-yl)sulfonyl)morpholine (52.5 mg, 0.20 mmol), Pd(PPh₃)₄ (23.1 mg, 0.02 mmol), K₂CO₃ (41.5 mg, 0.30 mmol), butylamine (116.8 mg, 1.60 mmol) and water (0.5 mL) were added sequentially. The resulting mixture was heated to 150° C. for 30 min under Microwave irradiation. The mixture was diluted with EtOAc (15 mL) and washed with water (2×). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was purified on ISCO and HPLC to give the title compound as a white solid (27.4 mg, 28%) and (1r,4r)-4-((2-(butylamino)pyrimidin-4-yl)amino)cyclohexanol (25.7 mg, 49%). ¹H NMR (400 MHz, CDCl₃) δ 10.65 (d, J=7.1 Hz, 1H), 9.46 (t, J=5.4 Hz, 1H), 8.87 (d, J=2.2 Hz, 1H), 8.31 (s, 1H), 8.10 (dd, J=8.6, 2.3 Hz, 1H), 7.77 (d, J=8.7 Hz, 1H), 4.19-4.09 (m, 1H), 3.84-3.68 (m, 5H), 3.51-3.44 (m, 2H), 3.15-3.06 (m, 4H), 2.86-2.66 (m, 3H), 2.28-2.15 (m, 2H), 2.13-2.01 (m, 2H), 1.72-1.61 (m, 2H), 1.56-1.36 (m, 6H), 0.96 (t, J=7.4 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 159.4, 156.9, 153.1, 146.6, 142.8, 136.8, 130.2, 118.9, 103.4, 69.2, 66.0, 49.7, 45.8, 41.3, 33.3, 31.0, 29.5, 20.1, 13.7; MS m/z 491.30 [M+H]⁺.

Table 4 describes compounds prepared following procedures described in Example 4 (General Procedure C), using appropriate reagents.

Physical Data Com- Mer MS m/z (M + 1) or/and ¹H Structure pound_ID IC₅₀ NMR 1

UNC1899A ++++ ¹H NMR (400 MHz, CDCl₃) δ 10.74 (d, J = 7.2 Hz, 1H), 9.09 (t, J = 5.4 Hz, 1H), 8.97 (d, J = 2.0 Hz, 1H), 8.47 (d, J = 11.7 Hz, 1H), 8.25-8.14 (m, 1H), 7.83 (t, J = 7.1 Hz, 1H), 5.27-5.16 (m, 1H), 4.19-4.03 (m, 4H), 3.82-3.75 (m, 1H), 3.52- 3.42 (m, 2H), 2.90 (t, J = 5.5 Hz, 2H), 2.66 (t, J = 12.7 Hz, 2H), 2.29-2.00 (m, 4H), 1.72-1.60 (m, 5H), 1.52-1.37 (m, 12H), 1.16-1.03 (m, 2H), 0.97 (t, J = 7.3 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 159.5, 156.4, 154.8, 152.9, 145.9, 142.7, 136.1, 134.7, 119.3, 103.7, 79.9, 69.2, 49.7, 48.6, 41.3, 36.6, 33.2, 31.0, 29.5, 28.4, 20.1, 13.7; MS m/z 618.40 [M + H]⁺. 2

UNC1918A ++++ ¹H NMR (400 MHz, CD₃OD + CDCl₃) δ 8.89 (t, J = 2.4 Hz, 1H), 8.39 (d, J = 17.0 Hz, 1H), 8.19-8.11 (m, 1H), 7.88 (t, J = 8.7 Hz, 1H), 5.08-4.93 (m, 1H), 4.25-4.11 (m, 1H), 4.12- 3.97 (m, 1H), 3.70-3.56 (m, 1H), 3.46-3.38 (m, 2H), 3.38-3.34 (m, 1H), 2.87-2.74 (m, 4H), 2.25-2.18 (m, 1H), 2.17- 2.08 (m, 2H), 2.03-1.95 (m, 1H), 1.93-1.85 (m, 2H), 1.79-1.68 (m, 2H), 1.64-1.56 (m, 3H), 1.48-1.33 (m, 6H), 0.92 (td, J = 7.4, 2.1 Hz, 3H); MS m/z 518.30 [M + H]⁺. 3

UNC1898A ++++ ¹H NMR (400 MHz, CDCl₃) δ 10.95 (d, J = 7.2 Hz, 1H), 9.03-8.85 (m, 2H), 8.33 (d, J = 14.4 Hz, 1H), 8.12 (dd, J = 8.6, 2.3 Hz, 1H), 7.70 (d, J = 8.6 Hz, 1H), 6.17 (d, J = 7.9 Hz, 1H), 4.24-3.70 (m, 9H), 3.51-3.40 (m, 2H), 2.92 (t, J = 12.1 Hz, 2H), 2.26-2.14 (m, 2H), 2.06 (t, J = 10.6 Hz, 4H), 1.70-1.59 (m, 2H), 1.54-1.35 (m, 14H), 0.96 (t, J = 7.4 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 164.0, 159.6, 155.3, 154.8, 152.9, 146.6, 141.6, 135.9, 128.0, 118.6, 104.1, 80.1, 69.2, 49.6, 47.7, 41.3, 33.2, 32.0, 31.0, 29.4, 28.4, 20.0, 13.7; MS m/z 568.40 [M + H]⁺. 4

UNC1917A +++ ¹H NMR (400 MHz, CDCl₃) δ 10.67 (s, 1H), 8.50 (d, J = 4.7 Hz, 1H), 8.12 (s, 1H), 7.79- 7.70 (m, 1H), 7.56 (d, J = 8.3 Hz, 1H), 7.24-7.14 (m, 1H), 4.13-4.04 (m, 1H), 3.79-3.71 (m, 1H), 3.48-3.38 (m, 2H), 2.26-2.13 (m, 2H), 2.11-2.01 (m, 2H), 1.69-1.60 (m, 2H), 1.54-1.34 (m, 6H), 0.95 (t, J =7.4 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 163.8, 159.9, 147.2, 137.5, 131.6, 118.9, 115.1, 104.4, 69.5, 49.6, 41.2, 33.6, 31.4, 29.8, 20.1, 13.8; MS m/z 342.25 [M + H]⁺.

Example 5 trans-4-((2-(Butylamino)-5-(5-fluoropyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol and trans-4-((2-(Butylamino)-5-(5-((4-methylpiperazin-1-yl)methyl)furan-2-yl)pyrimidin-4-yl)amino)cyclohexanol General Procedure D:

trans-4-((5-Bromo-2-(butylamino)pyrimidin-4-yl)amino)cyclohexanol

A solution of 5-bromo-2,4-dichloropyrimidine (34.2 g, 150 mmol) and 4-aminocyclohexanol (17.3 g, 150 mmol) in i-PrOH (300 mL) was added DIPEA (39.2 mL, 225 mmol). The reaction mixture was stirred for 12 h. Then the solvent was evaporated under reduced pressure and the residue was then redissolved in EtOAc and washed with brine. The organic layer was dried (Na₂SO₄) and concentrated to yield 4-((5-bromo-2-chloropyrimidin-4-yl)amino)cyclohexanol (46 g, 150 mmol) which was used without further purification.

To a solution of 4-((5-bromo-2-chloropyrimidin-4-yl)amino)cyclohexanol (46 g, 150 mmol) in toluene (150 mL) was added n-butylamine (150 mL, 1.5 mol). The reaction mixture was heated at 80° C. for 12 h. Then the solvent was evaporated under reduced pressure and the residue was then redissolved in EtOAc and washed with brine. The organic layer was dried (Na₂SO₄) and concentrated to yield trans-4-((5-bromo-2-(butylamino)pyrimidin-4-yl)amino)cyclohexanol (47.5 g, 92%). ¹H NMR (400 MHz, CDCl₃) δ 7.82 (s, 1H), 5.01-4.80 (m, 2H), 3.97-3.82 (m, 1H), 3.65 (tt, J=10.4, 4.2 Hz, 1H), 3.31 (dt, J=7.1, 6.1 Hz, 2H), 2.21 (s, 1H), 2.16-2.06 (m, 2H), 2.06-1.95 (m, 2H), 1.59-1.49 (m, 2H), 1.49-1.34 (m, 4H), 1.34-1.20 (m, 2H), 0.92 (t, J=7.3 Hz, 3H); ¹³C NMR (101 MHz, CDCl₃) δ 161.14 (s), 157.59 (s), 155.72 (s), 69.70 (s), 48.85 (s), 41.39 (s), 33.94 (s), 31.84 (s), 30.62 (s), 20.12 (s), 13.86 (s). MS m/z 343.0 [M+1]⁺;

trans-4-((2-(Butylamino)-5-(5-fluoropyridin-2-yl)pyrimidin-4-1 amino)cyclohexanol

A mixture of lithium (5-fluoropyridin-2-yl)trihydroxyborate (99 mg, 0.60 mmol), copper bromide (3.0 mg, 0.020 mmol), potassium carbonate (83.0 mg, 0.60 mmol), 4-((5-bromo-2-(butylamino)pyrimidin-4-yl)amino)cyclohexanol (68.7 mg, 0.20 mmol) and PdCl₂(dppf) (8.2 mg, 0.010 mmol) in a mixture of DMF and H₂O (2.0 mL/0.5 mL) was heated at 120° C. in the open air for 30 min, and then allowed to cool to room temperature. The insoluble material was removed by filtration through a short pad of celite, which was washed with DMF. The solvent was then removed under reduced pressure and the residue was Purified on ISCO to provide trans-4-((2-(butylamino)-5-(5-fluoropyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol (UNC2861A) (46 mg, 65%). ¹H NMR (400 MHz, CD₃OD) δ 8.54 (d, J=3.0 Hz, 1H), 8.26 (s, 1H), 7.93 (dd, J=9.0, 4.1 Hz, 1H), 7.80-7.71 (m, 1H), 4.20-4.05 (m, 1H), 3.67 (td, J=10.0, 5.1 Hz, 1H), 3.48 (s, 2H), 2.16 (d, J=8.5 Hz, 2H), 2.05-1.92 (m, 2H), 1.67 (dt, J=12.6, 7.5 Hz, 2H), 1.59-1.38 (m, 6H), 1.00 (t, J=7.4 Hz, 3H). LC-MS (ESI+): t_(R)=4.481 min, MS m/z 360.0 [M+1]⁺.

5-(2-(Butylamino)-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)furan-2-carbaldehyde

A mixture of palladium(II) acetate (2.9 mg, 0.013 mmol), potassium phosphate (186.8 mg, 0.88 mmol), trans-4-((5-bromo-2-(butylamino)pyrimidin-4-yl)amino)cyclohexanol (150 mg, 0.44 mmol), SPhos (9.1 mg, 0.022 mmol) and (5-formylfuran-2-yl)boronic acid (92.3 mg, 0.66 mmol) in butanol (2.5 mL) was degassed and heated under N₂ atmosphere and microwave irradiation at 150° C. in a 10 ml microwave tube for 20 min. The resulting mixture was diluted with water and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was purified on HPLC to provide 5-(2-(butylamino)-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)furan-2-carbaldehyde (50.1 mg, 32%). ¹H NMR (400 MHz, cdcl₃) δ 9.49 (s, 1H), 8.22 (s, 1H), 7.28 (d, J=3.8 Hz, 1H), 6.55 (d, J=3.8 Hz, 1H), 5.25-5.07 (m, 1H), 4.13-3.98 (m, 1H), 3.79-3.70 (m, 1H), 3.41 (dd, J=13.3, 6.9 Hz, 2H), 2.25-2.15 (m, 2H), 2.10-2.01 (m, 2H), 1.79-1.68 (m, 1H), 1.65-1.55 (m, 2H), 1.54-1.34 (m, 5H), 0.95 (t, J=7.3 Hz, 3H); ¹³C NMR (101 MHz, cdcl₃) δ 175.1, 161.9, 158.9, 157.7, 156.1, 150.4, 125.0, 104.4, 69.6, 48.6, 41.2, 33.6, 31.9, 30.2, 20.1, 13.9; MS m/z 359.20 [M+H]⁺.

trans-4-((2-(Butylamino)-5-(5-((4-methylpiperazin-1-yl)methyl)furan-2-yl)pyrimidin-4-yl)amino)cyclohexanol

A mixture of 1-methylpiperazine (29.3 mg, 0.29 mmol), 5-(2-(butylamino)-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)furan-2-carbaldehyde (35 mg, 0.098 mmol), acetic acid (28 mg, 0.29 mmol) and sodium triacetoxyborohydride (62.1 mg, 0.29 mmol) in DCM (10 mL) was stirred at room temperature for 2 h, then quenched with NaHCO₃ (sat.) and extracted with DCM (3×). The combined organic layers were washed with water and brine, dried (Na₂SO₄) and concentrated. The residue was purified on HPLC to provide trans-4-((2-(butylamino)-5-(5-((4-methylpiperazin-1-yl)methyl)furan-2-yl)pyrimidin-4-yl)amino)cyclohexanol (UNC2897A) (35.2 mg, 82%). ¹H NMR (400 MHz, cd₃od) δ 7.82 (s, 1H), 6.68 (d, J=3.4 Hz, 1H), 6.59 (d, J=3.4 Hz, 1H), 4.18-4.09 (m, 1H), 3.99 (s, 2H), 3.64-3.54 (m, 1H), 3.54-3.42 (m, 2H), 3.45-3.32 (m, 4H), 3.18-2.94 (m, 4H), 2.90 (s, 3H), 2.19-1.97 (m, 4H), 1.71-1.62 (m, 2H), 1.59-1.31 (m, 6H), 1.00 (t, J=7.4 Hz, 3H); ¹³C NMR (101 MHz, cd₃od) δ 160.6, 160.2, 149.5, 146.2, 139.4, 117.5, 114.6, 112.7, 109.6, 68.7, 52.5, 48.8, 42.0, 40.8, 33.3, 30.9, 29.0, 19.7, 12.7; MS m/z 443.35 [M+H]⁺.

Table 5 describes compounds prepared following procedures described in Example 5 (General Procedure D), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) or/and ¹H Structure Compound_ID IC₅₀ NMR 1

UNC3055A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.54 (dd, J = 5.5, 0.5 Hz, 1H), 8.38 (s, 1H), 8.02 (d, J = 1.5 Hz, 1H), 7.46 (dd, J = 5.5, 1.8 Hz, 1H), 4.23-4.05 (m, 1H), 3.72-3.59 (m, 1H), 3.49 (d, J = 7.7 Hz, 2H), 2.16 (d, J = 10.3 Hz, 2H), 2.02 (dd, J = 10.0, 3.7 Hz, 2H), 1.67 (tt, J = 8.1, 6.7 Hz, 2H), 1.59-1.36 (m, 5H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 376.0 [M + 1]⁺. 2

UNC2794A +++ ¹H NMR (400 MHz, CD₃OD) δ 9.14 (d, J = 1.2 Hz, 1H), 8.62 (dd, J = 2.6, 1.6 Hz, 1H), 8.59 (d, J = 2.6 Hz, 1H), 4.28- 4.10 (m, 1H), 3.66 (ddd, J = 13.8, 9.8, 3.9 Hz, 1H), 3.51 (s, 2H), 2.16 (d, J = 10.0 Hz, 2H), 2.02 (d, J = 12.3 Hz, 2H), 1.68 (dt, J = 12.7, 7.6 Hz, 2H), 1.61-1.35 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H). MS m/z 343.0 [M + 1]⁺. 3

UNC2860A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.55 (s, 1H), 8.40 (d, J = 8.8 Hz, 1H), 7.99 (dd, J = 8.6, 2.7 Hz, 2H), 7.95 (d, J = 8.2 Hz, 1H), 7.82 (ddd, J = 8.4, 7.0, 1.4 Hz, 1H), 7.63 (ddd, J = 8.1, 7.0, 1.1 Hz, 1H), 4.28- 4.11 (m, 1H), 3.83-3.66 (m, 1H), 3.50 (d, J = 16.0 Hz, 2H), 2.30 (d, J = 9.6 Hz, 2H), 2.09 (d, J = 9.7 Hz, 2H), 1.77-1.59 (m, 4H), 1.59-1.40 (m, 4H), 1.02 (t, J = 7.4 Hz, 3H). MS m/z 392.0 [M + H]⁺. 4

UNC2863A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.30 (s, 1H), 7.75 (s, 1H), 7.37-7.24 (m, 5H), 4.79 (s, 2H), 4.59 (s, 2H), 4.13 (s, 1H), 3.74-3.62 (m, 1H), 3.53 (d, J = 30.8 Hz, 2H), 2.16 (d, J = 7.7 Hz, 2H), 2.02 (d, J = 12.3 Hz, 2H), 1.74-1.61 (m, 2H), 1.59-1.36 (m, 6H), 1.00 (t, J = 7.3 Hz, 3H). MS m/z 468.0 [M + 1]⁺. 5

UNC2250B ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.78 (d, J = 1.8 Hz, 1H), 8.45 (s, 1H), 8.15 (dd, J = 8.5, 2.3 Hz, 1H), 8.04 (d, J = 8.5 Hz, 1H), 4.48 (s, 2H), 4.22- 4.13 (m, 1H), 4.05 (s, 2H), 3.81 (s, 2H), 3.66 (dd, J = 10.0, 4.9 Hz, 1H), 3.46 (d, J = 34.9 Hz, 4H), 3.26-3.17 (m, 2H), 2.18 (d, J = 11.2 Hz, 2H), 2.08-1.97 (m, 2H), 1.68 (dd, J = 8.2, 6.0 Hz, 2H), 1.59-1.39 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H). ¹³C NMR (101 MHz, CD₃OD) δ 173.60 (s), 159.49 (s), 154.02 (s), 149.84 (s), 141.27 (s), 140.70 (s), 125.88 (s), 123.30 (s), 120.06 (s), 68.45 (s), 63.48 (s), 57.10 (s), 51.52 (s), 49.93 (s), 40.86 (s), 32.85 (s), 30.74 (s), 29.19 (s), 19.68 (s), 12.72 (s). MS m/z 441.0 [M + 1]⁺. 6

UNC2432A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.73 (d, J = 1.8 Hz, 1H), 8.41 (s, 1H), 8.09 (dd, J = 8.5, 2.3 Hz, 1H), 7.99 (d, J = 8.5 Hz, 1H), 4.32 (s, 2H), 4.22- 4.05 (m, 1H), 3.74-3.61 (m, 1H), 3.47 (m, 2H), 3.22-3.13 (m, 1H), 2.18 (dd, J = 23.9, 11.4 Hz, 4H), 2.00 (dd, J = 13.3, 6.8 Hz, 2H), 1.90 (d, J = 12.6 Hz, 2H), 1.67 (m, 4H), 1.56-1.31 (m, 8H), 1.32-1.19 (m, 2H), 1.04-0.92 (t, J = 4 Hz, 3H). MS m/z 453.0 [M +1]⁺. 7

UNC2422A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.78 (d, J = 2.0 Hz, 1H), 8.43 (s, 1H), 8.16 (dd, J = 8.5, 2.3 Hz, 1H), 8.01 (d, J = 8.5 Hz, 1H), 4.50 (s, 2H), 4.19- 4.10 (m, 1H), 3.75-3.69 (m, 1H), 3.68-3.62 (m, 2H), 3.57- 3.41 (m, 4H), 2.47-2.34 (m, 4H), 2.15 (d, J = 12.5 Hz, 2H), 2.05-1.96 (m, 2H), 1.70-1.60 (m, 2H), 1.46 (ddd, J = 15.6, 14.9, 7.4 Hz, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 475.0 [M + 1]⁺. 8

UNC3021A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.54 (d, J = 2.9 Hz, 1H), 8.27 (s, 1H), 7.93 (dd, J = 9.0, 4.1 Hz, 1H), 7.75 (td, J = 8.7, 2.9 Hz, 1H), 3.56 (d, J = 6.5 Hz, 2H), 3.48 (s, 2H), 3.11- 3.01 (m, 1H), 2.08 (d, J = 10.5 Hz, 2H), 1.95 (d, J = 12.4 Hz, 2H), 1.77 (s, 1H), 1.65 (dt, J = 14.9, 7.4 Hz, 2H), 1.42 (qd, J = 14.5, 5.2 Hz, 4H), 1.29-1.13 (m, 2H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 373.0 [M + 1]⁺. 9

UNC2405A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.87 (s, 1H), 8.45 (s, 1H), 8.25 (d, J = 7.7 Hz, 1H), 8.01 (d, J = 8.4 Hz, 1H), 4.62 (s, 2H), 4.22-4.07 (m, 1H), 3.91 (m, 3H), 3.71-3.44 (m, 8H), 2.98 (s, 3H), 2.38 (s, 2H), 2.14 (d, J = 9.9 Hz, 2H), 2.01 (d, J = 12.9 Hz, 2H), 1.65 (m, 2H), 1.48 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 468.0 [M + 1]⁺. 10

UNC2490A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.78 (s, 1H), 8.43 (s, 1H), 8.15 (d, J = 8.1 Hz, 1H), 8.01 (d, J = 8.3 Hz, 1H), 4.50 (s, 2H), 4.20-4.10 (m, 1H), 3.66 (ddd, J = 12.4, 10.8, 7.5 Hz, 1H), 3.61-3.41 (m, 4H), 3.17 (dd, J = 42.2, 4.4 Hz, 2H), 2.25-2.10 (m, 4H), 2.01 (d, J = 11.8 Hz, 4H), 1.71-1.58 (m, 2H), 1.58-1.36 (m ,6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 425.0 [M + 1]⁺. 11

UNC2550A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.72 (d, J = 1.9 Hz, 1H), 8.43 (s, 1H), 8.08 (dd, J = 8.5, 2.3 Hz, 1H), 8.00 (d, J = 8.5 Hz, 1H), 4.20 (s, 2H), 4.18- 4.11 (m, 1H), 3.90-3.80 (m, 1H), 3.70-3.62 (m, 1H), 3.49 (s, 2H), 2.40-2.31 (m, 2H), 2.30-2.23 (m, 2H), 2.16 (d, J = 11.0 Hz, 2H), 2.04-1.98 (m, 2H), 1.96-1.86 (m, 2H), 1.66 (dt, J = 12.6, 7.6 Hz, 2H), 1.55-1.39 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 425.0 [M + 1]⁺. 12

UNC2491A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.11 (s, 1H), 8.69 (s, 1H), 8.23 (d, J = 26.9 Hz, 2H), 4.62 (s, 2H), 4.13 (s, 1H), 3.71- 3.43 (m, 3H), 2.94 (s, 1H), 2.22-1.89 (m, 4H), 1.67 (s, 2H), 1.59-1.31 (m, 6H), 1.11 (s, 2H), 0.98 (t, J = 6.9 Hz, 5H). MS m/z 411.0 [M + 1]⁺. 13

UNC2489A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.13 (s, 1H), 8.73 (s, 1H), 8.23 (s, 2H), 4.53 (s, 2H), 4.13 (s, 1H), 3.73 (dd, J = 10.9, 5.3 Hz, 1H), 3.68-3.46 (m, 3H), 2.21 (s, 2H), 2.14-1.94 (m, 4H), 1.87 (s, 4H), 1.64 (d, J = 34.4 Hz, 4H), 1.59-1.29 (m, 6H), 0.98 (t, J = 6.9 Hz, 3H). MS m/z 439.0 [M + 1]⁺. 14

UNC2547A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.76 (d, J = 1.9 Hz, 1H), 8.42 (s, 1H), 8.13 (dd, J = 8.5, 2.3 Hz, 1H), 8.01 (d, J = 8.5 Hz, 1H), 4.32 (d, J = 7.5 Hz, 2H), 4.15 (ddd, J = 14.4, 9.0, 3.8 Hz, 1H), 3.69-3.59 (m, 1H), 3.56-3.41 (m, 2H), 3.00 (t, J = 7.2 Hz, 2H), 2.16 (d, J = 10.8 Hz, 2H), 2.08-1.95 (m, 2H), 1.66 (dt, J = 12.6, 7.6 Hz, 2H), 1.58-1.36 (m, 6H), 1.20- 1.11 (m, 1H), 0.98 (td, J = 7.4, 2.8 Hz, 3H), 0.78-0.62 (m, 2H), 0.43 (tt, J = 14.6, 7.3 Hz, 2H). MS m/z 425.0 [M + 1]⁺. 15

UNC2488A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 1.5 Hz, 1H), 8.44 (s, 1H), 8.16-8.07 (m, 1H), 8.03 (d, J = 8.5 Hz, 1H), 4.43 (s, 2H), 4.15 (dd, J = 12.3, 8.4 Hz, 1H), 3.69-3.62 (m, 1H), 3.48 (d, J = 10.6 Hz, 2H), 2.90 (s, 6H), 2.16 (d, J = 10.2 Hz, 2H), 2.01 (d, J = 11.0 Hz, 2H), 1.72-1.61 (m, 2H), 1.56-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 399.0 [M + 1]⁺. 16

UNC2549A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.73 (d, J = 1.8 Hz, 1H), 8.43 (s, 1H), 8.15-8.04 (m, 1H), 8.00 (d, J = 8.5 Hz, 1H), 4.30 (s, 2H), 4.15 (ddd, J = 14.3, 9.0, 3.8 Hz, 1H), 3.72- 3.61 (m, 1H), 3.47 (d, J = 10.5 Hz, 2H), 3.20-3.11 (m, 2H), 2.16 (d, J = 10.9 Hz, 2H), 2.01 (dd, J = 9.9, 3.8 Hz, 2H), 1.72-1.59 (m, 2H), 1.55-1.40 (m, 6H), 1.36 (t, J = 7.3 Hz, 3H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 399.0 [M + 1]⁺. 17

UNC2546A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 1.9 Hz, 1H), 8.42 (s, 1H), 8.13 (dd, J = 8.5, 2.3 Hz, 1H), 8.01 (d, J = 8.5 Hz, 1H), 4.36 (s, 2H), 4.20- 4.08 (m, 1H), 3.89-3.80 (m, 2H), 3.66 (d, J = 4.0 Hz, 1H), 3.49 (s, 2H), 3.23-3.14 (m, 2H), 2.16 (d, J = 10.6 Hz, 2H), 2.07-1.92 (m, 2H), 1.66 (dt, J = 12.6, 7.6 Hz, 2H), 1.59-1.32 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 415.0 [M + 1]⁺. 18

UNC2571A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.01-8.91 (m, 2H), 8.44- 8.31 (m, 3H), 8.06 (t, J = 10.8 Hz, 1H), 7.27-7.04 (m, 2H), 4.76 (s, 2H), 4.65-4.53 (m, 2H), 4.17-4.11 (m, 1H), 3.72- 3.58 (m, 2H), 3.56-3.47 (m, 1H), 2.13 (d, J = 10.4 Hz, 2H), 2.01 (d, J = 7.4 Hz, 2H), 1.66 (dt, J = 12.6, 7.6 Hz, 2H), 1.59-1.36 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 462.0 [M + 1]⁺. 19

UNC2572A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.91 (s, 1H), 8.43-8.28 (m, 2H), 8.07 (d, J = 8.4 Hz, 1H), 7.65-7.55 (m, 2H), 7.50-7.38 (m, 3H), 4.48 (s, 2H), 4.37 (s, 2H), 4.16-4.05 (m, 1H), 3.63 (ddd, J = 21.0, 15.6, 14.7 Hz, 1H), 3.55-3.43 (m, 2H), 2.11 (d, J = 11.8 Hz, 2H), 2.00 (d, J = 10.4 Hz, 2H), 1.71-1.61 (m, 2H), 1.46 (ddd, J = 22.3, 18.0, 9.7 Hz, 6H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 461.0 [M + 1]⁺. 20

UNC2621A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.30 (s, 1H), 8.10-7.98 (m, 1H), 7.89 (d, J = 8.0 Hz, 1H), 7.60 (d, J = 7.4 Hz, 1H), 4.52 (s, 2H), 4.14 (tt, J = 11.2, 3.9 Hz, 1H), 3.66 (ddd, J = 14.6, 10.4, 4.2 Hz, 1H), 3.48 (dd, J = 7.9, 6.2 Hz, 2H), 2.94-2.83 (m, 1H), 2.20 (d, J = 10.8 Hz, 2H), 2.05 (d, J = 10.4 Hz, 2H), 1.69 (dd, J = 12.2, 4.8 Hz, 2H), 1.51 (ddd, J = 22.6, 19.3, 9.9 Hz, 6H), 1.01 (t, J = 7.4 Hz, 3H), 0.98-0.91 (m, 4H). MS m/z 411.0 [M + 1]⁺. 21

UNC2622A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.32 (s, 1H), 8.07 (t, J = 7.9 Hz, 1H), 7.94 (d, J = 8.0 Hz, 1H), 7.78 (d, J = 7.5 Hz, 1H), 4.63 (s, 2H), 4.12 (dd, J = 9.6, 5.7 Hz, 1H), 3.88-3.62 (m, 9H), 3.50 (s, 2H), 3.00 (s, 3H), 2.17 (d, J = 10.7 Hz, 2H), 2.06 (d, J = 10.4 Hz, 2H), 1.68 (dt, J = 14.9, 7.5 Hz, 4H), 1.44 (dt, J = 21.9, 11.0 Hz, 4H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 454.0 [M + 1]⁺. 22

UNC2552A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.77 (d, J = 1.9 Hz, 1H), 8.45 (s, 1H), 8.14 (dd, J = 8.5, 2.2 Hz, 1H), 8.03 (d, J = 8.5 Hz, 1H), 4.42 (s, 2H), 4.19- 4.11 (m, 1H), 3.71-3.61 (m, 1H), 3.50 (d, J = 11.7 Hz, 4H), 3.03 (td, J = 12.3, 2.5 Hz, 2H), 2.17 (d, J = 10.9 Hz, 2H), 1.99 (m, 5H), 1.89-1.74 (m, 3H), 1.72-1.59 (m, 2H), 1.59-1.39 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 439.0 [M + 1]⁺. 23

UNC2251B ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.74 (d, J = 1.7 Hz, 1H), 8.39 (s, 1H), 8.12 (dd, J = 8.5, 2.1 Hz, 1H), 7.97 (d, J = 8.5 Hz, 1H), 4.31-4.19 (m, 2H), 4.16 (ddd, J = 14.4, 9.0, 3.9 Hz, 1H), 3.74-3.38 (m, 9H), 3.28-3.11 (m, 2H), 2.97 (s, 3H), 2.17 (d, J = 10.6 Hz, 2H), 2.10-1.95 (m, 2H), 1.67 (dt, J = 12.6, 7.6 Hz, 2H), 1.59-1.36 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H). MS m/z 454.0 [M + 1]⁺. 24

UNC3125A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.30 (s, 1H), 8.07 (t, J = 7.9 Hz, 1H), 7.93 (d, J = 8.1 Hz, 1H), 7.72 (d, J = 7.5 Hz, 1H), 4.56 (s, 2H), 4.15 (td, J = 7.5, 3.7 Hz, 1H), 3.96 (d, J = 59.6 Hz, 4H), 3.71-3.62 (m, 1H), 3.51 (s, 6H), 2.17 (d, J = 10.8 Hz, 2H), 2.05 (d, J = 10.5 Hz, 2H), 1.66 (dt, J = 22.6, 11.0 Hz, 4H), 1.50-1.36 (m, 4H), 1.01 (t, J = 7.4 Hz, 3H). MS m/z 441.0 [M + 1]⁺. 25

UNC2862A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.61 (s, 1H), 8.22 (d, J = 7.4 Hz, 1H), 7.98-7.88 (m, 2H), 4.27 (d, J = 13.6 Hz, 2H), 4.13 (s, 1H), 3.80-3.64 (m, 3H), 3.62-3.49 (m, 4H), 3.42 (d, J = 11.5 Hz, 2H), 2.01 (s, 3H), 1.68 (dt, J = 14.5, 7.3 Hz, 2H), 1.59-1.25 (m, 6H), 1.00 (t, J = 7.3 Hz, 3H). MS m/z 440.0 [M + 1]⁺. 26

UNC2606A ++++ ¹H NMR (400 MHz, CD₃OD) δ 9.02 (d, J = 2.2 Hz, 1H), 8.43 (s, 1H), 8.31 (dd, J = 8.6, 2.3 Hz, 1H), 7.99 (d, J = 8.5 Hz, 1H), 4.22-4.11 (m, 2H), 3.98 (d, J = 6.8 Hz, 1H), 3.72- 3.62 (m, 2H),3.58 (dd, J = 15.5, 6.3 Hz, 2H), 3.53-3.41 (m, 2H), 3.18 (dd, J = 13.3, 10.6 Hz, 2H), 2.88 (s, 3H), 2.26 (d, J = 14.9 Hz, 2H), 2.17 (d, J = 11.8 Hz, 2H), 2.01 (d, J = 14.1 Hz, 2H), 1.93 (dd, J = 12.2, 3.3 Hz, 2H), 1.71-1.58 (m, 2H), 1.59-1.40 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 482.0 [M + 1]⁺. 27

UNC3027A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.74 (d, J = 2.0 Hz, 1H), 8.42 (d, J = 2.3 Hz, 1H), 8.03 (dt, J = 15.3, 5.3 Hz, 2H), 4.22-4.10 (m, 1H), 3.95 (s, 1H), 3.71-3.41 (m, 8H), 3.26- 3.17 (m, 2H), 2.95 (s, 3H), 2.16 (d, J = 10.4 Hz, 2H), 2.01 (d, J = 10.6 Hz, 2H), 1.66 (dt, J = 14.9, 7.4 Hz, 2H), 1.61- 1.32 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 468.0 [M + 1]⁺. 28

UNC2915A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.71 (s, 1H), 8.43 (s, 1H), 8.00 (s, 2H), 4.64 (s, 1H), 4.20-4.11 (m, 1H), 3.74-3.43 (m, 6H), 3.23 (s, 1H), 3.00 (d, J = 14.4 Hz, 3H), 2.90 (s, 3H), 2.32-1.97 (m, 8H), 1.68 (dt, J = 14.9, 7.6 Hz, 2H), 1.59-1.36 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H). MS m/z 496.0 [M + 1]⁺. 29

UNC3056A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.71-8.57 (m, 1H), 8.33 (s, 1H), 7.96 (dd, J = 8.8, 2.5 Hz, 1H), 7.89 (d, J = 8.8 Hz, 1H), 4.22-4.05 (m, 1H), 3.77-3.61 (m, 1H), 3.49 (s, 2H), 2.16 (d, J = 10.6 Hz, 2H), 2.08-1.95 (m, 2H), 1.67 (dt, J = 12.7, 7.6 Hz, 2H), 1.59-1.33 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 376.0 [M + 1]⁺. 30

UNC2795A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.71 (s, 1H), 8.29 (s, 1H), 8.11 (d, J = 8.0 Hz, 1H), 7.95 (d, J = 8.3 Hz, 1H), 4.14 (td, J = 10.5, 5.4 Hz, 1H), 3.99-3.58 (m, 12H), 3.50 (s, 2H), 3.38- 3.31 (m, 1H), 3.04 (s, 3H), 2.13 (d, J = 10.2 Hz, 2H), 2.01 (d, J = 10.5 Hz, 2H), 1.67 (dt, J = 14.9, 7.5 Hz, 2H), 1.61- 1.35 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 468.0 [M + 1]⁺. 31

UNC2793A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.74 (d, J = 1.6 Hz, 1H), 8.38 (s, 1H), 8.09-7.95 (m, 1H), 7.91 (d, J = 8.5 Hz, 1H), 4.15 (td, J = 10.4, 5.3 Hz, 1H), 4.04 (s, 2H), 3.77-3.37 (m, 9H), 3.25-3.07 (m, 3H), 2.96 (s, 3H), 2.17 (d, J = 10.2 Hz, 2H), 2.07-1.97 (m, 2H), 1.67 (dt, J = 12.7, 7.6 Hz, 2H), 1.62-1.36 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 478.0 [M + 1]⁺. 32

UNC2792A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.63 (d, J = 1.5 Hz, 1H), 8.26 (s, 1H), 8.02 (d, J = 8.4 Hz, 1H), 7.91 (d, J = 8.4 Hz, 1H), 4.19-4.11 (m, 1H), 4.05- 3.41 (m, 11H), 3.41-3.34 (m, 2H), 3.02 (s, 3H), 2.88 (t, J = 7.6 Hz, 2H), 2.29-2.20 (m, 2H), 2.19-2.08 (m, 2H), 2.07- 1.98 (m, 2H), 1.71-1.61 (m, 2H), 1.61-1.36 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 482.0 [M + 1]⁺. 33

UNC2777A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.90 (d, J = 2.5 Hz, 1H), 8.26 (s, 1H), 8.19 (dd, J = 8.9, 2.5 Hz, 1H), 7.87 (d, J = 8.9 Hz, 1H), 4.14 (dd, J = 12.4, 8.5 Hz, 1H), 3.65 (ddd, J = 21.9, 14.7, 6.2 Hz, 2H), 3.52- 3.40 (m, 2H), 3.12 (dd, J = 13.1, 10.5 Hz, 2H), 2.91 (s, 3H), 2.80-2.72 (m, 1H), 2.18 (t, J = 14.9 Hz, 4H), 2.03 (d, J = 11.5 Hz, 4H), 1.75-1.59 (m, 2H), 1.58-1.36 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 482.0 [M + 1]⁺. 34

UNC2710A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 8.06 (d, J = 2.7 Hz, 1H), 7.98 (s, 1H), 7.83 (d, J = 8.9 Hz, 1H), 7.64 (d, J = 8.8 Hz, 1H), 4.13 (dt, J = 10.5, 8.6 Hz, 1H), 3.74-3.56 (m, 1H), 3.48 (d, J = 1.6 Hz, 2H), 2.19-1.95 (m, 7H), 1.74-1.62 (m, 2H), 1.61-1.38 (m, 6H), 1.00 (dt, J = 7.8, 6.9 Hz, 3H). MS m/z 399.0 [M + 1]⁺. 35

UNC2711A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.80 (d, J = 2.2 Hz, 1H), 8.21 (s, 1H), 8.08 (dd, J = 8.9, 2.6 Hz, 1H), 7.78 (d, J = 8.9 Hz, 1H), 4.14-4.02 (m, 1H), 3.74-3.56 (m, 1H), 3.45 (s, 2H), 2.16 (d, J = 11.4 Hz, 2H), 2.07-1.95 (m, 2H), 1.86-1.74 (m, 1H), 1.72-1.59 (m, 2H), 1.46 (ddd, J = 14.9, 10.9, 8.3 Hz, 6H), 1.04-0.84 (m, 7H). MS m/z 425.0 [M + 1]⁺. 36

UNC2790A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.16 (dd, J = 8.9, 2.6 Hz, 1H), 8.04-7.96 (m, 1H), 7.82 (d, J = 8.9 Hz, 1H), 7.60 (d, J = 8.8 Hz, 1H), 4.13 (dd, J = 10.0, 4.0 Hz, 2H), 3.66 (dd, J = 13.7, 4.5 Hz, 2H), 3.47 (d, J = 1.6 Hz, 3H), 2.44-1.88 (m, 11H), 1.75-1.58 (m, 3H), 1.56-1.36 (m, 6H), 1.00 (td, J = 7.3, 1.1 Hz, 4H). MS m/z 439.0 [M + 1]⁺. 37

UNC2791A ++++ ¹H NMR (400 MHz, CD₃OD) 8.82 (d, J = 2.2 Hz, 1H), 8.24-8.15 (m, 1H), 7.83 (d, J = 8.9 Hz, 1H), 7.56 (d, J = 8.8 Hz, 1H), 4.14 (dd, J = 9.1, 5.3 Hz, 1H), 3.77-3.59 (m, 1H), 3.47 (d, J = 1.5 Hz, 2H), 2.85 (dd, J = 15.8, 7.8 Hz, 1H), 2.16 (s, 2H), 2.08-1.91 (m, 4H), 1.89-1.72 (m, 4H), 1.72- 1.59 (m, 4H), 1.61-1.36 (m, 6H), 1.00 (dd, J = 8.3, 6.5 Hz, 3H). MS m/z 453.0 [M + 1]⁺. 38

UNC2713A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.99 (d, J = 2.1 Hz, 1H), 8.32 (dd, J = 8.9, 2.6 Hz, 1H), 8.28 (s, 1H), 8.03-7.94 (m, 2H), 7.90 (d, J = 8.9 Hz, 1H), 7.62 (ddd, J = 6.6, 3.8, 1.3 Hz, 1H), 7.58-7.51 (m, 2H), 4.20- 4.10 (m, 1H), 3.68 (td, J = 10.1, 4.9 Hz, 1H), 3.48 (d, J = 1.7 Hz, 2H), 2.19 (d, J = 10.5 Hz, 2H), 2.03 (d, J = 11.4 Hz, 2H), 1.68 (dt, J = 12.7, 7.6 Hz, 2H), 1.61-1.38 (m, 6H), 1.01 (t, J = 9.7 Hz, 3H). MS m/z 461.0 [M + 1]⁺. 39

UNC2712A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.86-8.74 (m, 1H), 8.23 (s, 1H), 8.15 (dd, J = 8.9, 2.6 Hz, 1H), 7.82 (d, J = 8.7 Hz, 1H), 4.14 (td, J = 10.7, 5.4 Hz, 1H), 3.77-3.61 (m, 1H), 3.56-3.41 (m, 2H), 2.41 (ddd, J = 11.8, 7.7, 3.4 Hz, 1H), 2.16 (d, J = 12.3 Hz, 2H), 2.02 (d, J = 11.2 Hz, 2H), 1.87 (dd, J = 23.7, 8.8 Hz, 3H), 1.69 (ddd, J = 15.8, 14.9, 9.7 Hz, 3H), 1.61- 1.23 (m, 8H), 1.00 (t, J = 7.4 Hz, 3H). MS m/z 467.0 [M + 1]⁺. 40

UNC2898A +++ ¹H NMR (400 MHz, CD₃OD) δ 7.84 (s, 1H), 6.83 (d, J = 3.5 Hz, 1H), 6.73 (d, J = 3.4 Hz, 1H), 4.49 (s, 2H), 4.19-4.08 (m, 1H), 4.06-3.74 (m, 4H), 3.62-3.53 (m, 1H), 3.52-3.45 (m, 2H), 2.11-1.96 (m, 4H), 1.70-1.61 (m, 2H), 1.59-1.47 (m, 2H), 1.48-1.32 (m, 4H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 430.30 [M + H]⁺. 41

UNC2899A +++ ¹H NMR (400 MHz, CD₃OD) δ 7.84 (s, 1H), 6.83 (d, J = 3.5 Hz, 1H), 6.73 (d, J = 3.4 Hz, 1H), 4.52 (s, 2H), 4.18-4.09 (m, 1H), 3.63-3.39 (m, 7H), 2.45-2.29 (m, 4H), 2.19-1.94 (m, 4H), 1.72-1.60 (m, 2H), 1.60-1.48 (m, 2H), 1.46-1.32 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 464.30 [M + H]⁺. 42

UNC2900A +++ ¹H NMR (400 MHz, CD₃OD) δ 7.84 (s, 1H), 6.79 (d, J = 3.4 Hz, 1H), 6.71 (d, J = 3.4 Hz, 1H), 4.66 (t, J = 11.1 Hz, 4H), 4.57 (s, 2H), 4.18-4.09 (m, 1H), 3.63-3.54 (m, 1H), 3.54- 3.40 (m, 2H), 2.11-1.95 (m, 4H), 1.69-1.62 (m, 2H), 1.60- 1.49 (m, 2H), 1.48-1.33 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 436.30 [M + H]⁺. 43

UNC2902A ¹H NMR (400 MHz, CDCl₃) δ 9.49 (s, 1H), 8.22 (s, 1H), 7.28 (d, J = 3.8 Hz, 1H), 6.55 (d, J = 3.8 Hz, 1H), 5.25-5.07 (m, 1H), 4.13-3.98 (m, 1H), 3.79-3.70 (m, 1H), 3.41 (dd, J = 13.3, 6.9 Hz, 2H), 2.25-2.15 (m, 2H), 2.10-2.01 (m, 2H), 1.79-1.68 (m, 1H), 1.65-1.55 (m, 2H), 1.54-1.34 (m, 5H), 0.95 (t, J = 7.3 Hz, 3H); ¹³C NMR (101 MHz, CDCl3) δ 175.1, 161.9, 158.9, 157.7, 156.1, 150.4, 125.0, 104.4, 69.6, 48.6, 41.2, 33.6, 31.9, 30.2, 20.1, 13.9; MS m/z 359.20 [M + H]⁺. 44

UNC3181A ¹H NMR (400 MHz, CD₃OD) δ 8.02 (d, J = 9.5 Hz, 1H), 7.26 (t, J = 3.9 Hz, 1H), 6.86- 6.78 (m, 1H), 5.00 (ddd, J = 11.6, 8.0, 3.6 Hz, 1H), 4.30- 4.20 (m, 1H), 4.19-4.11 (m, 1H), 3.63-3.55 (m, 2H), 3.54- 3.41 (m, 2H), 3.23-3.10 (m, 2H), 2.94-2.84 (m, 3H), 2.65 (s, 1H), 2.25-2.13 (m, 4H), 2.10-1.99 (m, 2H), 1.98- 1.85 (m, 2H), 1.72-1.61 (m, 4H), 1.57-1.51 (m, 1H), 1.50-1.34 (m, 3H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 471.30 [M + 1]⁺. 45

UNC4103A ¹H NMR (400 MHz, CD₃OD) δ 8.76 (d, J = 4.0 Hz, 1H), 8.44 (s, 1H), 8.14 (dd, J = 4.0 Hz, J = 8.0 Hz, 1H), 8.02 (d, J = 8.0 Hz, 1H), 4.34 (s, 2H), 4.19- 4.13 (m, 1H), 3.75-3.67 (m, 1H), 3.55-3.45 (m, 2H), 2.76 (s, 3H), 2.22-2.14 (m, 2H), 2.06-1.97 (m, 5H), 1.82-1.76 (m, 3H), 1.75-1.64 (m, 5H), 1.63-1.40 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 519.75 [M + H]⁺. 46

UNC4104A ¹H NMR (400 MHz, CD₃OD) δ 8.82 (d, J = 2.0 Hz, 1H), 8.43 (s, 1H), 8.19 (dd, J = 2.0 Hz, J = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.57 (s, 2H), 4.30- 4.12 (m, 1H), 3.90-3.75 (m, 1H), 3.72-3.63 (m, 2H), 3.55- 3.45 (m, 2H), 2.97 (s, 6H), 2.70-2.57 (m, 2H), 2.52-2.35 (m, 2H), 2.22-2.13 (m, 2H), 2.06-1.97 (m, 2H), 1.71-1.64 (m, 2H), 1.60-1.40 (m, 6H), 1.01 (t, J = 8.0 Hz, 3H). MS m/z 468.66 [M + H]⁺. 47

UNC4161A ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 2.0 Hz, 1H), 8.41 (s, 1H), 8.12 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.99 (d, J = 8.0 Hz, 1H), 4.34 (s, 2H), 4.20- 4.09 (m, 1H), 3.70-3.63 (m, 1H), 3.55-3.44 (m, 2H), 2.20- 2.12 (m, 2H), 2.06-2.98 (m, 2H), 1.69-1.62 (m, 2H), 1.58- 1.38 (m, 6H), 1.04 (s, 9H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 441.64 [M + H]⁺. 48

UNC4162A ¹H NMR (400 MHz, CD₃OD) δ 8.79 (dd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, 1H), 8.43 (s, 1H), 8.12 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.44 (s, 2H), 4.18-4.10 (m, 1H), 3.70-3.62 (m, 1H), 3.55- 3.43 (m, 2H), 2.20-2.11 (m, 2H), 2.06-1.98 (m, 2H), 1.70- 1.62 (m, 2H), 1.60-1.40 (m, 6H), 1.37 (t, J = 8.0 Hz, 3H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 427.61 [M + 1]⁺. 49

UNC4163A ¹H NMR (400 MHz, CD₃OD) δ 8.79 (d, J₁ = 2.0 Hz, 1H), 8.40 (s, 1H), 8.16 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.97 (d, J = 8.0 Hz, 1H), 4.36 (s, 2H), 4.18-4.10 (m, 1H), 4.10-4.05 (m, 2H), 3.98-3.87 (m, 1H), 3.70-3.62 (m, 2H), 3.54-3.42 (m, 2H), 2.82 (s, 3H), 2.51- 2.25 (m, 7H), 2.20-2.19 (m, 3H), 2.05-1.96 (m, 2H), 1.70- 1.61 (m, 2H), 1.60-1.39 (m, 6H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 494.70 [M + H]⁺. 50

UNC4165A ¹H NMR (400 MHz, CD₃OD) δ 8.81 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.41 (s, 1H), 8.19 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.98 (d, J = 8.0 Hz, 1H), 4.44 (s, 2H), 4.18-4.10 (m, 1H), 3.98-3.85 (m, 2H), 3.75- 3.62 (m, 2H), 3.54-3.42 (m, 2H), 2.80 (s, 3H), 2.78-2.73 (m, 2H), 2.52-2.44 (m, 2H), 2.37-2.32 (m, 2H), 2.27-2.22 (m, 2H), 2.20-2.12 (m, 2H), 2.05-1.95 (m, 2H), 1.70-1.63 (m, 2H), 1.57-1.38 (m, 6H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 494.70 [M + H]⁺. 51

UNC4197A ¹H NMR (400 MHz, CD₃OD) δ 8.77 (d, J = 4.0 Hz, 1H), 8.43 (s, 1H), 8.87 (dd, J₁ = 4.0 Hz, J₂ = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.49 (s, 2H), 4.21- 4.10 (m, 1H), 3.72-3.62 (m, 1H), 3.61-3.51 (m, 4H), 3.25- 3.17 (m, 2H), 2.25-2.12 (m, 4H), 2.10-1.98 (m, 4H), 1.60- 1.53 (m, 2H), 1.53-1.38 (m, 4H), 0.82-0.70 (m, 1H), 0.53- 0.47 (m, 2H), 0.15-0.09 (m, 2H). MS m/z 437.60 [M + H]⁺. 52

UNC3668A ¹H NMR (400 MHz, CD₃OD) δ 8.84 (d, J = 4.0 Hz, 1H), 8.43-8.28 (m, 1H), 8.23 (d, J = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.52 (s, 2H), 4.22- 4.10 (m, 1H), 3.85-3.47 (m, 8H), 2.99 (s, 3H), 2.25-2.06 (m, 2H), 2.06-1.95 (m, 2H), 1.80-1.32 (m, 8H), 0.95 (t, J = 8.0 Hz, 3H), 0.93-0.77 (m, 4H). MS m/z 480.67 [M + H]⁺.

Example 6 trans-3-((2-(Butylamino)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclobutanol General Procedure E:

trans-3-((2-(Butylamino)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclobutanol

A solution of 2,4-dichloro-5-iodopyrimidine (456 mg, 2 mmol) and 3-aminocyclobutanol (183 mg, 2.1 mmol) in ^(i)PrOH (6.0 mL) was stirred under microwave irradiation at 80° C. for 20 min, then BuNH₂ (1.0 mL) was added. The resulting reaction mixture was stirred under microwave irradiation at 100° C. for 30 min, then quenched with brine and extracted with CH₂Cl₂ (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was the dissolved in a mixture of DMF/H₂O (8.0 mL/2.0 mL). To this solution was added lithium 2-pyridinyl trihydroxyborate (882 mmol, 6.0 mmol), copper bromide (57.4 mg, 0.40 mmol), Potassium carbonate (828 mg, 6.0 mmol) and PdCl₂(dppf) (164 mg, 0.20 mmol). The reaction mixture was heated at 120° C. for 30 min. Then it was diluted with EtOAc (15 mL) after cooled to room temperature. The suspension was filtered through a short pad of celite, which was washed with ethyl acetate. The filtrate was washed with water (2×30 mL), dried (MgSO₄) and concentrated. The residue was purified on the ISCO to provide trans-3-((2-(butylamino)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclobutanol (UNC2963A) (326 mg, 52% (over three steps)). ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J=5.1 Hz, 1H), 8.27 (s, 1H), 7.98 (d, J=8.2 Hz, 1H), 7.90 (d, J=8.2 Hz, 1H), 7.57-7.37 (m, 1H), 4.77-4.64 (m, 1H), 4.53-4.41 (m, 1H), 3.75-3.55 (m, 1H), 3.49 (s, 2H), 2.43 (t, J=6.2 Hz, 4H), 1.64 (dd, J=14.8, 7.5 Hz, 2H), 1.44 (dd, J=15.0, 7.4 Hz, 2H), 0.98 (t, J=7.4 Hz, 3H). MS m/z 314.0 [M+1]⁺;

Table 6 describes compounds prepared following procedures described in Example 6 (General Procedure E), using appropriate reagents.

Mer Physical Data Entry Structure Compound_ID IC₅₀ MS m/z (M + 1) or/and ¹H NMR 1

UNC2958A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 5.1 Hz, 1H), 8.27 (s, 1H), 8.07 (t, J = 7.9 Hz, 1H), 7.94 (d, J = 8.1 Hz, 1H), 7.58-7.47 (m, 1H), 4.22-4.04 (m, 1H), 3.75-3.53 (m, 1H), 3.48 (s, 2H), 2.84 (d, J = 7.0 Hz, 2H), 2.22 (d, J = 11.0 Hz, 2H), 1.95 (d, J = 12.5 Hz, 2H), 1.68 (ddd, J = 22.3, 10.9, 5.5 Hz, 3H), 1.59- 1.33 (m, 4H), 1.22 (dd, J = 25.7, 12.1 Hz, 2H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 355.0 [M + 1]⁺. 2

UNC2960A + ¹H NMR (400 MHz, CD₃OD) δ 8.76 (d, J = 5.2 Hz, 1H), 8.26 (t, J = 7.6 Hz, 1H), 8.17 (s, 1H), 8.00 (d, J = 8.1 Hz, 1H), 7.79-7.63 (m, 1H), 3.75-3.58 (m, 4H), 3.61-3.44 (m, 2H), 1.97-1.83 (m, 2H), 1.66 (dt, J = 14.9, 7.3 Hz, 2H), 1.44 (dq, J = 14.5, 7.3 Hz, 2H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 326.0 [M + 1]⁺; LC-MS (ESI+): t_(R) = 4.195 min, MS m/z 302.0 [M + 1]⁺. 3

UNC2964A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.68 (d, J = 5.1 Hz, 1H), 8.22 (s, 1H), 8.07 (t, J = 7.8 Hz, 1H), 7.92 (d, J = 8.2 Hz, 1H), 7.61-7.41 (m, 1H), 3.64 (t, J = 6.9 Hz, 2H), 3.55 (t, J = 6.3 Hz, 2H), 3.49-3.41 (m, 2H), 1.72 (dd, J = 14.4, 7.1 Hz, 2H), 1.68-1.62 (m, 2H), 1.58 (dt, J = 13.1, 6.7 Hz, 2H), 1.46 (ddd, J = 22.4, 13.0, 7.6 Hz, 4H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 330.0 [M + 1]⁺. 4

UNC3003A ¹H NMR (400 MHz, CD₃OD) δ 8.67 (dd, J = 4.3, 0.8 Hz, 1H), 8.05 (td, J = 7.8, 1.7 Hz, 1H), 7.95 (s, 1H), 7.68 (d, J = 7.8 Hz, 1H), 7.53 (dd, J = 7.6, 5.1 Hz, 1H), 3.71 (s, 4H), 3.50 (s, 2H), 3.24 (s, 4H), 1.65 (dt, J = 14.9, 7.2 Hz, 2H), 1.43 (dd, J = 15.0, 7.5 Hz, 2H), 0.97 (t, J = 7.4 Hz, 3H). MS m/z 313.0 [M + 1]⁺. 5

UNC2961A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.63 (d, J = 5.0 Hz, 1H), 8.38 (s, 1H), 8.07-7.88 (m, 2H), 7.47-7.40 (m, 1H), 4.47 (s, 1H), 3.72-3.55 (m, 1H), 3.47 (dd, J = 13.4, 4.0 Hz, 3H), 3.21 (d, J = 11.5 Hz, 2H), 2.36 (d, J = 11.1 Hz, 2H), 1.93 (dd, J = 21.0, 10.4 Hz, 2H), 1.66 (dt, J = 15.0, 7.4 Hz, 2H), 1.45 (dd, J = 15.0, 7.4 Hz, 2H), 0.99 (t, J = 7.3 Hz, 3H). MS m/z 327.0 [M + 1]⁺. 6

UNC2962A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 5.0 Hz, 1H), 8.30 (s, 1H), 8.01 (t, J = 7.7 Hz, 1H), 7.92 (d, J = 8.2 Hz, 1H), 7.55-7.40 (m, 1H), 3.67 (t, J = 16.8 Hz, 3H), 3.50 (s, 1H), 3.42 (d, J = 12.7 Hz, 2H), 2.99 (t, J = 11.7 Hz, 2H), 2.11 (d, J = 3.7 Hz, 1H), 2.02 (d, J = 13.8 Hz, 2H), 1.71-1.61 (m, 2H), 1.54 (d, J = 13.2 Hz, 2H), 1.45 (dd, J = 15.0, 7.5 Hz, 2H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 341.0 [M + 1]⁺. 7

UNC2996A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J = 5.0 Hz, 1H), 8.25 (s, 1H), 8.01-7.91 (m, 1H), 7.86 (d, J = 8.2 Hz, 1H), 7.44- 7.34 (m, 1H), 3.67 (dd, J = 8.9, 5.0 Hz, 2H), 3.60 (t, J = 6.4 Hz, 2H), 3.48 (d, J = 8.0 Hz, 2H), 1.84-1.72 (m, 2H), 1.71-1.56 (m, 4H), 1.43 (dd, J = 15.0, 7.5 Hz, 2H), 0.97 (d, J = 7.4 Hz, 3H). MS m/z 316.0 [M + 1]⁺. 8

UNC2997A + ¹H NMR (400 MHz, CD₃OD) δ 8.81 (d, J = 5.2 Hz, 1H), 8.36 (t, J = 7.7 Hz, 1H), 8.17 (s, 1H), 8.06 (d, J = 8.1 Hz, 1H), 7.88-7.74 (m, 1H), 3.78 (t, J = 5.2 Hz, 2H), 3.72 (d, J = 4.6 Hz, 2H), 3.51 (s, 2H), 1.66 (dt, J = 14.9, 7.4 Hz, 2H), 1.44 (dd, J = 15.0, 7.4 Hz, 2H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 288.0 [M + 1]⁺. 9

UNC2998A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.68 (d, J = 4.9 Hz, 1H), 8.39 (s, 1H), 8.07-7.92 (m, 2H), 7.58-7.38 (m, 3H), 6.83 (t, J = 6.0 Hz, 2H), 3.38 (d, J = 6.5 Hz, 2H), 1.59 (dd, J = 14.5, 7.3 Hz, 2H), 1.46- 1.32 (m, 2H), 0.93 (t, J = 7.3 Hz, 3H). MS m/z 336.0 [M + 1]⁺. 10

UNC3000A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.72 (d, J = 4.9 Hz, 1H), 8.55 (s, 1H), 7.98 (dd, J = 15.0, 5.8 Hz, 4H), 7.47 (dd, J = 8.8, 4.0 Hz, 3H), 3.53-3.38 (m, 2H), 1.68- 1.59 (m, 2H), 1.41 (d, J = 7.0 Hz, 2H), 1.28-1.13 (m, 2H), 0.95 (t, J = 8.0 Hz, 3H). MS m/z 335.0 [M + 1]⁺. 11

UNC2999A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.59 (d, J = 4.9 Hz, 1H), 8.32 (s, 1H), 7.91 (ddd, J = 20.9, 13.7, 5.0 Hz, 1H), 7.47-7.30 (m, 1H), 4.15 (d, J = 4.3 Hz, 2H), 3.47 (dd, J = 7.0, 3.8 Hz, 2H), 3.20 (s, 2H), 2.27 (s, 2H), 2.16 (s, 2H), 1.66 (dd, J = 14.5, 7.2 Hz, 2H), 1.59 (dd, J = 16.5, 7.4 Hz, 2H), 1.44 (td, J = 14.8, 7.3 Hz, 2H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 341.0 [M + 1]⁺. 12

UNC3001A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.67 (d, J = 5.0 Hz, 1H), 8.27 (s, 1H), 8.05 (dd, J = 11.1, 4.5 Hz, 1H), 7.94 (d, J = 8.1 Hz, 1H), 7.52 (dd, J = 7.2, 5.5 Hz, 1H), 3.59-3.46 (m, 4H), 3.07 (ddd, J = 11.9, 8.2, 4.0 Hz, 1H), 2.08 (d, J = 9.4 Hz, 2H), 1.96 (d, J = 12.2 Hz, 2H), 1.77 (d, J = 3.1 Hz, 1H), 1.66 (dt, J = 14.9, 7.4 Hz, 2H), 1.52-1.33 (m, 4H), 1.22 (dd, J = 24.8, 11.1 Hz, 2H), 0.99 (t, J = 7.4 Hz, 3H). MS m/z 355.0 [M + 1]⁺. 13

UNC2959A + ¹H NMR (400 MHz, CD₃OD) δ 8.65- 8.52 (m, 1H), 8.28 (s, 1H), 7.91 (dt, J = 18.9, 8.1 Hz, 2H), 7.50-7.34 (m, 1H), 4.20 (d, J = 3.6 Hz, 1H), 3.46 (s, 2H), 2.02 (s, 2H), 1.80 (s, 2H), 1.65 (dt, J = 14.8, 7.3 Hz, 3H), 1.43 (td, J = 14.8, 7.4 Hz, 7H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 326.0 [M + 1]⁺. 14

UNC3002A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.74 (d, J = 5.2 Hz, 1H), 8.25 (t, J = 7.5 Hz, 1H), 8.18 (s, 1H), 8.01 (d, J = 8.1 Hz, 1H), 7.76-7.58 (m, 1H), 4.82-4.73 (m, 1H), 4.37 (dt, J = 8.5, 2.9 Hz, 1H), 3.54 (d, J = 12.6 Hz, 2H), 2.38-2.23 (m, 1H), 2.19-2.11 (m, 1H), 2.10-2.01 (m, 1H), 1.86-1.77 (m, 1H), 1.67 (dt, J = 14.8, 7.2 Hz, 4H), 1.45 (dq, J = 14.5, 7.4 Hz, 2H), 0.98 (t, J = 7.4 Hz, 3H). MS m/z 328.0 [M + 1]⁺.

Example 7 trans-4-((2-(Methylamino)-5-(pyridin-2-0)pyrimidin-4-yl)amino)cyclohexanol General Procedure F:

trans-4-((5-Bromo-2-(methylthio)pyrimidin-4-yl)amino)cyclohexanol

A solution of 2,4-dichloro-5-iodopyrimidine (2.6 g, 10 mmol) and 4-aminocyclohexanol (1.27 g, 11 mmol) in ^(i)PrOH (60 mL) was stirred at room temperature overnight, then diluted with CH₂Cl₂ and washed by brine. The organic layer was dried (Na₂SO₄) and concentrated. The residue was purified on ISCO to afford trans-4-((5-bromo-2-(methylthio)pyrimidin-4-yl)amino)cyclohexanol as a white solid (3.19 g, >99%). ¹H NMR (400 MHz, CDCl₃) δ 8.04 (s, 1H), 5.10 (d, J=7.2 Hz, 1H), 3.97 (dtd, J=11.1, 7.3, 3.8 Hz, 1H), 3.74-3.59 (m, 1H), 2.13 (d, J=12.4 Hz, 2H), 2.02 (d, J=12.4 Hz, 2H), 1.58 (d, J 25.3 Hz, 1H), 1.44 (ddd, J=23.2, 12.9, 3.2 Hz, 2H), 1.30 (ddd, J=24.2, 12.8, 3.1 Hz, 2H). ¹³C NMR (101 MHz, cdcl₃) δ 170.33 (s), 156.85 (s), 155.07 (s), 99.73 (s), 69.70 (s), 49.15 (s), 33.78 (s), 30.41 (s), 14.34 (d, J=3.7 Hz). LC-MS (ESI+): t_(R)=5.104 min, MS m/z 318.0 [M+1]⁺;

trans-4-((2-(Methylthio)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol

A solution of trans-4-((5-bromo-2-(methylthio)pyrimidin-4-yl)amino)cyclohexanol (2.18 g, 6.36 mmol) in a mixture of DMF/H₂O (16.0 mL/4.0 mL) was added 2-pyridinyl trihydroxyborate lithium (2.80 g, 19.1 mmol), copper bromide (183 mg, 1.27 mmol), potassium carbonate (2.63 g, 19.1 mmol) were and PdCl₂(dppf) (519 mg, 0.64 mmol) at room temperature. The reaction mixture was heated at 120° C. for 30 min, and then diluted with EtOAc (15 mL) after cooled to room temperature. The resulting suspension was filtered through a short pad of celite, which was washed with ethyl acetate. The filtrate was washed with water (2×30 mL), dried (MgSO₄), and concentrated. The residue was purified by the flash chromatography to provide trans-4-((2-(methylthio)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol as a white solid (1.06 g, 53%). ¹H NMR (400 MHz, CD₃OD) δ 8.58-8.49 (m, 1H), 8.43 (s, 1H), 7.85 (ddd, J=10.0, 9.6, 5.0 Hz, 2H), 7.34-7.22 (m, 1H), 4.09 (dd, J=9.4, 5.3 Hz, 1H), 3.69-3.58 (m, 1H), 2.52 (s, 3H), 2.19-2.11 (m, 2H), 1.98 (dd, J=10.7, 7.7 Hz, 2H), 1.50-1.32 (m, 3H). ¹³C NMR (101 MHz, cd₃od) δ 170.96 (s), 158.47 (s), 154.56 (s), 152.22 (s), 147.21 (s), 137.25 (s), 121.55 (s), 119.78 (s), 108.55 (s), 68.89 (s), 33.02 (s), 29.75 (s), 12.66 (d, J=3.6 Hz).

trans-4-((2-(Methylamino)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol

A solution of trans-4-((2-(methylthio)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol (95 mg, 0.5 mmol) in THF (5 mL) was added mCPBA (130 mg, 0.75 mmol). The reaction mixture was stirred at room temperature for 2 h. Then methylamine (2 mmol) was added. The reaction mixture was heated under microwave irradiation at 150° C. for 30 min. The solvent was removed under reduced pressure. The residue was purified on ISCO to afford trans-4-((2-(methylamino)-5-(pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol (UNC3122A) as a light brown solid (120 mg, 80%). ¹H NMR (400 MHz, CD₃OD) δ 8.73 (d, J=4.5 Hz, 1H), 8.27-8.15 (m, 2H), 8.00 (d, J=8.1 Hz, 1H), 7.71-7.58 (m, 1H), 4.18 (s, 1H), 3.68-3.56 (m, 1H), 3.05 (s, 3H), 2.12 (s, 2H), 2.01 (d, J=10.6 Hz, 2H), 1.46 (dd, J=23.8, 12.8 Hz, 4H). LC-MS (ESI+): t_(R)=3.914 min, MS m/z 300.0 [M+1]⁺;

Table 7 describes compounds prepared following procedures described in Example 7 (General Procedure F), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) or/and ¹H Structure Compound_ID IC₅₀ NMR 1

UNC3123A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.82-8.70 (m, 1H), 8.32- 8.15 (m, 2H), 8.01 (d, J = 8.1 Hz, 1H), 7.76-7.64 (m, 1H), 4.23-4.10 (m, 1H), 3.69-3.55 (m, 1H), 3.53 (s, 2H), 2.12 (d, J = 11.5 Hz, 2H), 2.01 (d, J = 11.3 Hz, 2H), 1.58-1.36 (m, 4H), 1.30 (t, J = 7.2 Hz, 3H). MS m/z 314.0 [M + 1]⁺. 2

UNC3028A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.74 (dd, J = 23.7, 5.1 Hz, 1H), 8.31 (t, J = 7.7 Hz, 1H), 8.18 (s, 1H), 8.05 (t, J = 12.3 Hz, 1H), 7.79-7.67 (m, 1H), 4.20-4.01 (m, 1H), 3.61 (t, J = 6.3 Hz, 2H), 3.53 (s, 2H), 2.08 (t, J = 12.5 Hz, 2H), 2.00 (d, J = 10.3 Hz, 2H), 1.83-1.71 (m, 2H), 1.63 (dt, J = 13.0, 6.3 Hz, 2H), 1.53-1.35 (m, 4H). MS m/z 358.0 [M + 1]⁺. 3

UNC3024A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.70 (d, J = 4.8 Hz, 1H), 8.23 (s, 1H), 8.17 (t, J = 7.6 Hz, 1H), 7.97 (d, J = 8.1 Hz, 1H), 7.68-7.58 (m, 1H), 4.20- 4.10 (m, 1H), 3.68 (t, J = 6.1 Hz, 2H), 3.64-3.53 (m, 2H), 2.12 (d, J = 10.1 Hz, 2H), 1.99 (d, J = 10.2 Hz, 2H), 1.95- 1.80 (m, 2H), 1.45 (dd, J = 21.7, 11.6 Hz, 4H). MS m/z 330.0 [M + 1]⁺. 4

UNC3029A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.63 (d, J = 5.0 Hz, 1H), 8.37 (s, 1H), 7.97 (ddd, J = 21.5, 11.2, 4.9 Hz, 2H), 7.56 (d, J = 8.1 Hz, 2H), 7.52-7.38 (m, 3H), 7.27 (t, J = 7.4 Hz, 1H), 4.07 (ddd, J = 14.7, 9.3, 3.8 Hz, 1H), 3.64 (ddd, J = 14.3, 10.0, 4.1 Hz, 1H), 2.14 (dd, J = 12.9, 2.8 Hz, 2H), 2.00 (dd, J = 13.1, 3.3 Hz, 2H), 1.59-1.44 (m, 2H), 1.39 (ddd, J = 23.3, 12.8, 3.1 Hz, 2H). MS m/z 362.0 [M + 1]⁺. 5

UNC3025A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 5.1 Hz, 1H), 8.24 (s, 1H), 8.07 (dd, J = 11.1, 4.7 Hz, 1H), 7.92 (d, J = 8.2 Hz, 1H), 7.54 (dd, J = 7.1, 5.6 Hz, 1H), 7.35-7.16 (m, 5H), 4.12 (d, J = 3.9 Hz, 1H), 3.73 (s, 2H), 3.68-3.56 (m, 1H), 2.96 (t, J = 7.3 Hz, 2H), 2.13 (d, J = 10.0 Hz, 2H), 2.01 (d, J = 10.0 Hz, 2H), 1.59- 1.38 (m, 4H). MS m/z 390.0 [M + 1]⁺. 6

UNC3022A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 4.9 Hz, 1H), 8.25 (s, 1H), 8.05 (d, J = 7.8 Hz, 1H), 7.93 (d, J = 8.2 Hz, 1H), 7.58-7.46 (m, 1H), 4.22- 3.98 (m, 1H), 3.68-3.53 (m, 1H), 3.48 (s, 2H), 2.13 (d, J = 11.7 Hz, 2H), 2.00 (d, J = 11.0 Hz, 2H), 1.75-1.62 (m, 2H), 1.43 (ddd, J = 16.6, 14.1, 9.7 Hz, 8H), 0.94 (t, J = 6.9 Hz, 3H). MS m/z 356.0 [M + 1]⁺. 7

UNC3023A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.74 (d, J = 5.3 Hz, 1H), 8.28-8.18 (m, 2H), 8.00 (d, J = 8.1 Hz, 1H), 7.80-7.64 (m, 1H), 4.22-4.05 (m,1H), 3.77 (t, J = 5.4 Hz, 2H), 3.61 (dq, J = 15.8, 5.4 Hz, 3H), 2.10 (d, J = 9.9 Hz, 2H), 1.99 (d, J = 10.0 Hz, 2H), 1.44 (q, J = 11.8 Hz, 4H). MS m/z 330.0 [M + 1]⁺. 8

UNC3050A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.64 (d, J = 5.0 Hz, 1H), 8.28 (s, 1H), 8.07 (td, J = 8.0, 1.6 Hz, 1H), 7.93 (d, J = 8.2 Hz, 1H), 7.53 (dd, J = 7.4, 5.3 Hz, 1H), 7.41-7.31 (m, 4H), 7.26 (t, J = 6.8 Hz, 1H), 4.65 (s, 2H), 3.99 (s, 1H), 3.57 (s, 1H), 1.93 (d, J = 5.2 Hz, 4H), 1.47-1.31 (m, 4H). MS m/z 376.0 [M + 1]⁺. 9

UNC3051A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.77 (d, J = 5.1 Hz, 1H), 8.30 (td, J = 7.9, 1.5 Hz, 1H), 8.16 (s, 1H), 8.05 (d, J = 8.1 Hz, 1H), 7.75 (dd, J = 7.1, 5.9 Hz, 1H), 4.09 (dd, J = 12.4, 8.8 Hz, 1H), 3.71 (s, 2H), 3.59 (ddd, J = 9.8, 9.2, 4.1 Hz, 1H), 3.24 (s, 3H), 2.17-2.04 (m, 2H), 2.04-1.97 (m, 2H), 1.70 (dt, J = 15.2, 7.6 Hz, 2H), 1.61-1.32 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H). MS m/z 356.0 [M + 1]⁺. 10

UNC3052A + ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 5.1 Hz, 1H), 8.21 (s, 1H), 8.12-8.01 (m, 1H), 7.96 (d, J = 8.1 Hz, 1H), 7.53 (dd, J = 7.4, 5.3 Hz, 1H), 4.08 (td, J = 10.2, 4.8 Hz, 1H), 3.79 (s, 4H), 3.66-3.58 (m, 1H), 2.13 (d, J = 11.1 Hz, 2H), 2.05-1.92 (m, 2H), 1.84-1.69 (m, 6H), 1.56-1.36 (m, 4H). MS m/z 354.0 [M + 1]⁺. 11

UNC3053A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J = 5.0 Hz, 1H), 8.28 (s, 1H), 8.09-7.92 (m, 1H), 7.89 (d, J = 8.2 Hz, 1H), 7.44 (dd, J = 7.0, 5.5 Hz, 1H), 4.09 (t, J = 10.3 Hz, 1H), 3.89 (s, 1H), 3.65 (tt, J = 8.4, 4.1 Hz, 1H), 2.15 (d, J = 11.2 Hz, 2H), 2.02 (d, J = 11.9 Hz, 4H), 1.94-1.78 (m, 2H), 1.69 (d, J = 12.5 Hz, 1H), 1.62-1.20 (m, 9H). MS m/z 368.0 [M + 1]⁺. 12

UNC3054A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.67 (s, 1H), 8.23 (s, 1H), 8.11 (d, J = 7.4 Hz, 1H), 7.95 (d, J = 7.1 Hz, 1H), 7.56 (s, 1H), 4.24-4.07 (m, 2H), 3.69- 3.58 (m, 1H), 2.12 (d, J = 12.4 Hz, 2H), 2.00 (d, J = 9.9 Hz, 2H), 1.72-1.35 (m, 8H), 1.29 (d, J = 6.6 Hz, 3H), 0.97 (t, J = 7.3 Hz, 3H). MS m/z 356.0 [M + 1]⁺. 13

UNC3020A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.67 (d, J = 4.9 Hz, 1H), 8.24 (s, 1H), 8.10 (t, J = 7.7 Hz, 1H), 7.95 (d, J = 8.2 Hz, 1H), 7.61-7.46 (m, 1H), 4.20- 4.07 (m, 1H), 3.71-3.55 (m, 1H), 3.44 (s, 2H), 2.12 (d, J = 11.9 Hz, 2H), 2.07-1.91 (m, 2H), 1.80-1.61 (m, 2H), 1.59- 1.35 (m, 4H), 1.01 (t, J = 7.4 Hz, 3H). MS m/z 328.0 [M + 1]⁺.

Example 8 trans-4-((2-(Butylamino)-5-(4-(morpholinomethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol General Procedure G:

(2-Chloro-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)boronic acid

5-Bromo-2,4-dichloropyrimidine (51 g, 223.8 mmol) was dissolved in anhydrous dioxane (150 mL) at 0° C. Then trans-4-aminocyclohexanol (26.3 g, 228.3 mmol) was added in several portions, followed by the addition of DIEA (37.6 g, 290.9 mmol). The resulting mixture was stirred at 0° C. for 5 h and at room temperature for 3 h, quenched with water (100 mL) and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄), and concentrated. The residue was recrystallized from a mixture of EtOAc/hexane to provide trans-4-((5-bromo-2-chloropyrimidin-4-yl)amino)cyclohexanol (55 g) as white solid, which was used in the next step without further purification.

A mixture of trans-4-((5-bromo-2-chloropyrimidin-4-yl)amino)cyclohexanol (5.50 g, 17.94 mmol), bis(pinacolato)diboron (6.83 g, 26.90 mmol), Pd(dppf)₂Cl₂ (732 mg, 0.90 mmol) and KOAc (5.28 g, 53.80 mmol) in anhydrous dioxane (125 mL) was thoroughly degassed and heated under N₂ atmosphere at 90° C. for 75 min. The hot mixture was then filtered through a pad of celite and concentrated, the residue was purified on ISCO (to remove most of unreacted trans-4-((5-bromo-2-chloropyrimidin-4-yl)amino)cyclohexanol) followed by a further purification on the reversed ISCO (elute solvents containing 0.1% TFA) to provide 2-chloro-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)boronic acid (1.84 g, 36% over 3 steps). ¹H NMR (400 MHz, cd₃od) δ 7.98 (s, 1H), 3.99-3.90 (m, 1H), 3.64-3.56 (m, 1H), 2.07-2.00 (m, 2H), 2.00-1.91 (m, 2H), 1.48-1.34 (m, 4H); MS m/z 272.30 [M+H]⁺.

trans-4-((2-(Butylamino)-5-(4-(morpholinomethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol

A mixture of (2-chloro-4-((trans-4-hydroxycyclohexyl)amino) pyrimidin-5-yl)boronic acid (45 mg, 0.166 mmol), 4-((2-bromopyridin-4-yl)methyl)morpholine (85.2 mg, 0.33 mmol), Pd₂(dba)₃ (7.6 mg, 0.008 mmol), PCy₃ (6.9 mg, 0.025 mmol), K₃PO₄ (0.33 mL, 1M solution in deionized water) and butylamine (50 mg, 0.66 mmol) in a 10 mL microwave tube was degassed and filled with N2 (3×). The resulting mixture was heated at 120° C. under microwave irradiation for 20 min, then quenched with water, and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄), and concentrated. The residue was purified on HPLC to provide trans-4-((2-(butylamino)-5-(4-(morpholinomethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol (UNC3015A) (54.5 mg, 75%) as a white solid. ¹H NMR (400 MHz, cd₃od) δ 8.72-8.66 (m, 1H), 8.42-8.34 (m, 1H), 8.04 (s, 1H), 7.52-7.48 (m, 1H), 4.43 (s, 2H), 4.19-4.09 (m, 1H), 3.93-3.83 (m, 3H), 3.70-3.60 (m, 1H), 3.56-3.42 (m, 2H), 3.37-3.30 (m, 3H), 2.20-2.11 (m, 2H), 2.07-1.95 (m, 2H), 1.70-1.62 (m, 2H), 1.55-1.36 (m, 5H), 0.99 (t, J=7.4 Hz, 3H); MS m/z 441.30 [M+H]⁺.

Table 8 describes compounds prepared following procedures described in Example 8 (General Procedure G), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) or/and ¹H Structure Compound_ID IC₅₀ NMR 1

UNC3014A ¹H NMR (400 MHz, CD3OD) δ 8.76-8.71 (m, 1H), 8.25- 8.19 (m, 1H), 7.76-7.71 (m, 1H), 7.64-7.57 (m, 1H), 4.38 (s, 2H), 4.20-4.07 (m, 1H), 3.91-3.74 (m, 4H), 3.55-3.45 (m, 2H), 3.24-3.08 (m, 4H), 2.16-2.03 (m, 1H), 2.02-1.87 (m, 3H), 1.75-1.53 (m, 3H), 1.54-1.40 (m ,3H), 1.40-1.28 (m, 3H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 441.30 [M + H]⁺. 2

UNC3041A +++ ¹H NMR (400 MHz, CD3OD) δ 8.32 (d, J = 1.4 Hz, 1H), 8.02 (s, 1H), 7.92 (d, J = 1.4 Hz, 1H), 4.15-4.06 (m, 1H), 3.66-3.59 (m, 1H), 3.50-3.36 (m, 2H), 2.17-2.08 (m, 2H), 2.03-1.94 (m, 2H), 1.69-1.58 (m, 2H), 1.54-1.35 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 358.25 [M + H]⁺. 3

UNC3042A ++++ ¹H NMR (400 MHz, dmso-d6) δ 10.50 (d, J = 6.6 Hz, 1H), 8.66 (s, 1H), 8.41 (d, J = 9.2 Hz, 1H), 8.33-8.27 (m, 1H), 8.25 (d, J = 9.2 Hz, 1H), 4.10- 3.96 (m, 2H), 3.51-3.46 (m, 2H), 3.41-3.35 (m, 2H), 2.07- 1.96 (m, 2H), 1.89-1.81 (m, 2H), 1.61-1.51 (m, 2H), 1.48- 1.39 (m, 2H), 1.37-1.25 (m, 4H), 0.91 (t, J = 7.3 Hz, 3H); MS m/z 387.25 [M + H]⁺. 4

UNC3043A +++ ¹H NMR (400 MHz, CD3OD) δ 7.87 (s, 1H), 7.76 (s, 1H), 4.14-4.06 (m, 1H), 4.04 (s, 3H), 3.62-3.55 (m, 1H), 3.52- 3.35 (m, 2H), 2.17-2.08 (m, 2H), 2.04-1.95 (m, 2H), 1.69- 1.57 (m, 2H), 1.50-1.35 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 388.30 [M + H]⁺. 5

UNC3044A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.41 (s, 1H), 8.20 (d, J = 10.1 Hz, 1H), 7.71 (d, J = 10.0 Hz, 1H), 4.22-4.11 (m, 1H), 3.78-3.65 (m, 4H), 3.66-3.57 (m, 1H), 3.55-3.42 (m, 2H), 2.25-2.08 (m, 6H), 2.07-1.95 (m, 2H), 1.72-1.61 (m, 2H), 1.57-1.32 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 412.30 [M + H]⁺. 6

UNC3045A +++ ¹H NMR (400 MHz, CD3OD) δ 8.07 (s, 1H), 7.71 (s, 1H), 4.14-4.04 (m, 1H), 3.71-3.63 (m, 1H), 3.45 (s, 2H), 2.75 (s, 3H), 2.19-2.11 (m, 2H), 2.03- 1.95 (m, 2H), 1.70-1.59 (m, 2H), 1.54-1.36 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 362.20 [M + H]⁺. 7

UNC3046A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.24 (s, 1H), 7.69 (s, 1H), 4.80 (s, 2H), 4.15-4.07 (m, 1H), 3.69-3.60 (m, 1H), 3.53- 3.41 (m, 2H), 2.20-2.11 (m, 2H), 2.05-1.96 (m, 2H), 1.70- 1.60 (m, 2H), 1.55-1.36 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 378.30 [M + H]⁺. 8

UNC3047A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.31 (s, 1H), 7.85 (d, J = 3.4 Hz, 1H), 7.60 (d, J = 3.4 Hz, 1H), 4.17-4.09 (m, 1H), 3.69- 3.62 (m, 1H), 3.55-3.41 (m, 2H), 2.21-2.12 (m, 2H), 2.05- 1.97 (m, 2H), 1.70-1.61 (m, 2H), 1.56-1.37 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 348.30 [M+ H]⁺. 9

UNC3048A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.45-8.39 (m, 1H), 8.14- 8.10 (m, 1H), 7.75-7.70 (m, 1H), 5.17-5.02 (m, 1H), 4.39- 4.23 (m, 1H), 4.22-4.13 (m, 1H), 3.72-3.61 (m, 1H), 3.57- 3.42 (m, 2H), 2.75-2.67 (m, 3H), 2.27-2.12 (m, 3H), 2.08- 1.93 (m, 2H), 1.74-1.64 (m, 3H), 1.58-1.51 (m, 1H), 1.48- 1.41 (m, 3H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 357.30 [M + H]⁺. 10

UNC3049A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.32 (s, 1H), 8.07 (d, J = 9.5 Hz, 1H), 7.28 (d, J = 9.5 Hz, 1H), 4.21-4.14 (m, 1H), 4.12 (s, 3H), 3.70-3.61 (m, 1H), 3.57-3.39 (m, 2H), 2.16 (d, J = 10.9 Hz, 2H), 2.02 (d, J = 9.8 Hz, 2H), 1.73-1.62 (m, 2H), 1.60-1.49 (m, 2H), 1.49-1.35 (m, 4H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 373.30 [M + H]⁺. 11

UNC3069A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.20 (s, 1H), 7.82 (d, J = 9.6 Hz, 1H), 7.09 (d, J = 9.6 Hz, 1H), 4.19-4.08 (m, 1H), 3.69- 3.60 (m, 1H), 3.52-3.37 (m, 2H), 2.73-2.64 (m, 1H), 2.16 (d, J = 10.8 Hz, 2H), 2.03 (d, J = 11.3 Hz, 2H), 1.72-1.59 (m, 2H), 1.56-1.40 (m, 5H), 0.99 (t, J = 7.4 Hz, 3H), 0.91-0.81 (m, 2H), 0.61-0.51 (m, 2H); MS m/z 398.30 [M + H]⁺. 12

UNC3071A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.23 (s, 1H), 7.92 (d, J = 9.9 Hz, 1H), 7.44 (d, J = 9.9 Hz, 1H), 4.21-4.13 (m, 1H), 3.77- 3.67 (m, 4H), 3.69-3.63 (m, 1H), 3.64-3.53 (m, 4H), 3.55- 3.42 (m, 2H), 2.16 (d, J = 10.5 Hz, 2H), 2.03 (d, J = 9.7 Hz, 2H), 1.72-1.62 (m, 2H), 1.61- 1.51 (m, 2H), 1.49 (s, 9H), 1.47-1.38 (m, 3H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 527.40 [M + H]⁺. 13

UNC3072A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.49 (d, J = 1.1 Hz, 1H), 8.18 (s, 1H), 6.85 (d, J = 0.7 Hz, 1H), 4.15-4.07 (m, 1H), 3.67-3.59 (m, 1H), 3.55-3.41 (m, 2H), 2.17-2.08 (m, 2H), 2.05-1.96 (m, 2H), 1.70-1.61 (m, 2H), 1.55-1.35 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 358.25 [M + H]⁺. 14

UNC3074A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.90 (d, J = 1.6 Hz, 1H), 8.50 (d, J = 1.5 Hz, 1H), 8.33 (s, 1H), 4.18-4.10 (m, 1H), 3.68-3.60 (m, 1H), 3.49 (s, 2H), 2.62 (s, 3H), 2.20-2.09 (m, 2H), 2.06-1.95 (m, 2H), 1.71-1.63 (m, 2H), 1.54-1.37 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 389.20 [M + H]⁺. 15

UNC3126A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.55 (s, 1H), 8.12 (s, 1H), 6.80 (s, 1H), 4.16-4.04 (m, 1H), 3.69-3.57 (m, 1H), 3.56- 3.38 (m, 2H), 3.00 (s, 3H), 2.21-2.07 (m, 2H), 2.07-1.91 (m, 2H), 1.76-1.57 (m, 3H), 1.55-1.33 (m, 5H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 372.30 [M + H]⁺. 16

UNC3113A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.52 (s, 1H), 8.12 (s, 1H), 6.77 (s, 1H), 4.15-4.06 (m, 1H), 3.66-3.58 (m, 1H), 3.53- 3.40 (m, 3H), 2.20-2.07 (m, 2H), 2.05-1.94 (m, 2H), 1.75- 1.57 (m, 3H), 1.58-1.30 (m, 6H), 1.26 (t, J = 7.2 Hz, 3H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 386.30 [M + H]⁺. 17

UNC3114A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.79 (d, J = 1.1 Hz, 1H), 8.44 (s, 1H), 7.28 (s, 1H), 4.17-4.08 (m, 1H), 4.03 (s, 3H), 3.71-3.62 (m, 1H), 3.54- 3.44 (m, 2H), 2.21-2.12 (m, 2H), 2.06-1.99 (m, 2H), 1.71- 1.62 (m, 2H), 1.60-1.50 (m, 2H), 1.50-1.39 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 373.25 [M + H]⁺. 18

UNC3115A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.29 (s, 1H), 8.13 (s, 1H), 7.89 (s, 1H), 4.16-4.09 (m, 1H), 3.65-3.58 (m, 1H), 3.57- 3.51 (m, 4H), 3.52-3.42 (m, 2H), 2.23-2.15 (m, 2H), 2.15- 2.08 (m, 4H), 2.07-2.01 (m, 2H), 1.71-1.63 (m, 2H), 1.44 (tt, J = 10.6, 5.4 Hz, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 412.30 [M + H]⁺. 19

UNC3116A +++ ¹H NMR (400 MHz, CD3OD) δ 8.33 (d, J = 21.0 Hz, 1H), 7.83 (d, J = 11.4 Hz, 1H), 7.59 (d, J = 1.4 Hz, 1H), 4.25-4.04 (m, 2H), 3.87 (s, 3H), 3.64- 3.53 (m, 1H), 3.53-3.40 (m, 2H), 2.21-2.11 (m, 2H), 2.11- 2.03 (m, 2H), 2.03-1.94 (m, 2H), 1.72-1.58 (m, 3H), 1.53- 1.32 (m, 5H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 345.30 [M + H]⁺. 20

UNC3117A ++ ¹H NMR (400 MHz, CD3OD) δ 7.83 (s, 1H), 7.62-7.58 (m, 1H), 7.45-7.36 (m, 7H), 7.29- 7.21 (m, 4H), 7.21-7.14 (m, 4H), 4.13-4.05 (m, 1H), 3.68- 3.58 (m, 1H), 3.51-3.36 (m, 2H), 2.94-2.81 (m, 1H), 2.19- 2.05 (m, 2H), 2.04-1.94 (m, 2H), 1.94-1.82 (m, 2H), 1.82- 1.72 (m, 1H), 1.70-1.59 (m, 2H), 1.56-1.35 (m, 6H), 1.04- 0.94 (m, 3H); MS m/z 573.35 [M + H]⁺. 21

UNC3118A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.57 (s, 1H), 8.27-8.21 (m, 1H), 7.20 (d, J = 6.4 Hz, 1H), 4.20-4.12 (m, 1H), 3.69-3.61 (m, 1H), 3.57-3.44 (m, 2H), 2.12 (d, J = 11.9 Hz, 2H), 2.05 (d, J = 11.0 Hz, 2H), 1.73- 1.58 (m, 4H), 1.50-1.34 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 358.30 [M + H]⁺. 22

UNC3119A ++ ¹H NMR (400 MHz, CD3OD) δ 7.99 (d, J = 2.9 Hz, 1H), 7.92 (d, J = 2.9 Hz, 1H), 7.83 (s, 1H), 4.18-4.09 (m, 1H), 3.59-3.44 (m, 3H), 2.06-1.93 (m, 4H), 1.73-1.63 (m, 2H), 1.54-1.20 (m, 7H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 358.30 [M + H]⁺. 23

UNC3120A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.33 (s, 1H), 7.87 (d, J = 3.4 Hz, 1H), 7.62 (d, J = 3.4 Hz, 1H), 4.20-4.10 (m, 1H), 3.72- 3.63 (m, 1H), 3.64-3.51 (m, 2H), 2.24-2.13 (m, 2H), 2.08- 1.97 (m, 2H), 1.61-1.54 (m, 3H), 1.52-1.42 (m, 3H), 0.81- 0.72 (m, 1H), 0.55-0.46 (m, 2H), 0.17-0.08 (m, 2H); MS m/z 360.20 [M + H]⁺. 24

UNC3130A +++ ¹H NMR (400 MHz, CD3OD) δ 8.48 (s, 1H), 7.56 (s, 1H), 4.15-4.06 (m, 1H), 3.74-3.64 (m, 1H), 3.58-3.39 (m, 2H), 2.65 (s, 3H), 2.60 (s, 3H), 2.20 (d, J = 10.8 Hz, 2H), 2.03 (d, J = 11.0 Hz, 2H), 1.71-1.61 (m, 2H), 1.60-1.38 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 403.25 [M + H]⁺. 25

UNC3121A ++++ ¹H NMR (400 MHz, CD3OD) δ 8.26 (s, 1H), 7.73 (s, 1H), 4.19-4.09 (m, 1H), 3.92 (s, 2H), 3.72-3.62 (m, 1H), 3.59- 3.36 (m, 4H), 2.89 (s, 3H), 2.77-2.32 (m, 3H), 2.16 (d, J = 10.8 Hz, 2H), 2.02 (d, J = 11.3 Hz, 2H), 1.80-1.58 (m, 3H), 1.63-1.25 (m, 7H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 460.30 [M + H]⁺. 26

UNC3134A ¹H NMR (400 MHz, CD3OD) δ 8.39 (s, 1H), 8.31 (s, 1H), 4.19-4.10 (m, 1H), 3.70-3.63 (m, 1H), 3.55-3.45 (m, 2H), 2.17 (d, J = 11.2 Hz, 2H), 2.03 (d, J = 11.0 Hz, 2H), 1.71- 1.62 (m, 2H), 1.60-1.36 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 391.20 [M + H]⁺. 27

UNC3135A ¹H NMR (400 MHz, CD3OD) δ 8.30 (s, 1H), 7.42 (s, 1H), 4.71 (d, J = 0.9 Hz, 2H), 4.18- 4.10 (m, 1H), 3.74-3.64 (m, 1H), 3.58-3.39 (m, 2H), 2.22- 2.12 (m, 2H), 2.07-1.98 (m, 2H), 1.72-1.63 (m, 2H), 1.62- 1.51 (m, 2H), 1.51-1.38 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 378.20 [M + H]⁺. 28

UNC3136A ¹H NMR (400 MHz, CD3OD) δ 8.36 (s, 1H), 8.26 (s, 1H), 4.15-4.07 (m, 1H), 3.71-3.62 (m, 1H), 3.55-3.45 (m, 2H), 2.17 (d, J = 11.6 Hz, 2H), 2.04 (d, J = 10.4 Hz, 2H), 1.71- 1.59 (m, 4H), 1.50-1.38 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 391.20 [M + H]⁺. 29

UNC3137A ¹H NMR (400 MHz, CD3OD) δ 8.16 (s, 1H), 7.95 (s, 1H), 7.83 (s, 1H), 4.20-4.10 (m, 1H), 3.75-3.67 (m, 1H), 3.65- 3.55 (m, 1H), 3.54-3.41 (m, 2H), 2.23-2.15 (m, 2H), 2.07- 1.98 (m, 4H), 1.90-1.82 (m, 2H), 1.75-1.62 (m, 3H), 1.55- 1.28 (m, 11H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 440.40 [M + H]⁺. 30

UNC3138A ¹H NMR (400 MHz, CD3OD) δ 8.27-8.21 (m, 2H), 8.21 (s, 1H), 4.15-4.07 (m, 1H), 3.88- 3.81 (m, 4H), 3.65-3.57 (m, 5H), 3.56-3.42 (m, 2H), 2.21- 2.12 (m, 2H), 2.07-1.99 (m, 2H), 1.71-1.63 (m, 2H), 1.50- 1.37 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 428.30 [M + H]⁺. 31

UNC3139A ¹H NMR (400 MHz, CD3OD) δ 8.39 (s, 1H), 8.37 (s, 1H), 4.28-4.10 (m, 1H), 3.77-3.63 (m, 1H), 3.59-3.40 (m, 2H), 2.26-2.12 (m, 2H), 2.11-1.99 (m, 2H), 1.73-1.62 (m, 2H), 1.63-1.52 (m, 2H), 1.52-1.39 (m, 4H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 392.20 [M + H]⁺. 32

UNC3140A ¹H NMR (400 MHz, CD3OD) δ 8.18 (s, 1H), 7.52 (d, J = 1.2 Hz, 1H), 4.17-4.08 (m, 1H), 3.70-3.61 (m, 1H), 3.58-3.37 (m, 2H), 2.51 (d, J = 1.1 Hz, 3H), 2.24-2.09 (m, 2H), 2.07- 1.93 (m, 2H), 1.72-1.58 (m, 2H), 1.53-1.40 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 362.20 [M + H]⁺. 33

UNC3141A ¹H NMR (400 MHz, CD3OD) δ 8.75 (s, 1H), 8.47 (s, 1H), 8.32 (d, J = 8.0 Hz, 1H), 8.23 (s, 2H), 8.20 (d, J = 7.8 Hz, 1H), 7.70-7.63 (m, 1H), 4.24- 4.13 (m, 1H), 3.74-3.63 (m, 1H), 3.51 (t, J = 7.0 Hz, 2H), 2.21 (d, J = 9.8 Hz, 2H), 2.06 (d, J = 9.9 Hz, 2H), 1.74-1.63 (m, 2H), 1.64-1.54 (m, 2H), 1.53-1.39 (m, 4H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 463.30 [M + H]⁺. 34

UNC3146A ¹H NMR (400 MHz, CD3OD) δ 8.33 (s, 1H), 7.88 (d, J = 3.4 Hz, 1H), 7.62 (d, J = 3.4 Hz, 1H), 4.20-4.12 (m, 1H), 3.71- 3.64 (m, 1H), 3.62 (t, J = 6.3 Hz, 2H), 3.58-3.47 (m, 2H), 2.22-2.13 (m, 2H), 2.06-1.97 (m, 2H), 1.90-1.70 (m, 3H), 1.68-1.60 (m, 2H), 1.57-1.41 (m, 4H); MS m/z 364.20 [M + H]⁺. 35

UNC3149A ¹H NMR (400 MHz, CD3OD) δ 8.45 (s, 1H), 8.26 (d, J = 0.9 Hz, 1H), 4.23-4.11 (m, 1H), 3.75-3.65 (m, 1H), 3.51 (t, J = 6.7 Hz, 2H), 2.26-2.15 (m, 2H), 2.07-1.95 (m, 2H), 1.73- 1.62 (m, 2H), 1.56-1.39 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 416.20 [M + H]⁺. 36

UNC3180A ¹H NMR (400 MHz, CD3OD) δ 8.46 (s, 1H), 8.32-8.26 (m, 1H), 4.20-4.10 (m, 1H), 3.71- 3.62 (m, 1H), 3.51 (t, J = 6.7 Hz, 2H), 2.17 (d, J = 11.1 Hz, 2H), 2.02 (d, J = 10.9 Hz, 2H), 1.72-1.62 (m, 2H), 1.58- 1.39 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 416.20 [M + H]⁺. 37

UNC3182A ¹H NMR (400 MHz, CD3OD) δ 8.46 (d, J = 0.9 Hz, 1H), 8.21 (s, 1H), 8.11-8.05 (m, 2H), 7.24-7.18 (m, 2H), 6.82 (s, 1H), 5.08-5.01 (m, 1H), 4.29-4.22 (m, 1H), 3.55- 3.44 (m, 2H), 2.28-2.10 (m, 4H), 1.80-1.59 (m, 6H), 1.49- 1.42 (m, 2H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 480.30 [M + H]⁺. 38

39

40

UNC3331A ¹H NMR (400 MHz, d- DMSO) δ 9.47 (s, 1H), 8.50 (s, 1H), 8.31 (s, 1H), 8.05-7.97 (m, 1H), 4.00-3.07 (m, 7H), 2.10-1.93 (m, 2H), 1.82-1.76 (m, 2H), 1.54-1.41 (m, 2H), 1.41-1.18 (m, 5H), 0.98-0.93 (m, 3H). MS m/z 392.20 [M + H]⁺. 41

UNC3201A ¹H NMR (400 MHz, CD3OD) δ 8.54 (s, 1H), 8.08 (br, 1H), 6.78 (s, 1H), 4.15-4.06 (m, 1H), 3.67-3.57 (m, 1H), 3.55- 3.40 (m, 4H), 2.14-2.05 (m, 2H), 2.04-1.97 (m, 2H), 1.70- 1.63 (m, 4H), 1.55-1.36 (m, 10H), 1.00 (d, J = 8.0 Hz, 3H), 0.97-0.92 (m, 3H). MS m/z 428.59 [M + H]⁺. 42

UNC3191A ¹H NMR (400 MHz, CD3OD) δ 8.54 (s, 1H), 8.11 (br, 1H), 6.79 (s, 1H), 4.16-4.05 (m, 1H), 3.68-3.55 (m, 1H), 3.54- 3.39 (m, 4H), 2.14-2.05 (m, 2H), 2.04-1.96 (m, 2H), 1.70- 1.60 (m, 4H), 1.55-1.35 (m, 8H), 0.99 (dt, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 3H). MS m/z 413.56 [M + H]⁺. 43

UNC3192A ¹H NMR (400 MHz, CD3OD) δ 8.55 (s, 1H), 8.08 (br, 1H), 6.76 (s, 1H), 4.50-4.30 (m, 1H), 4.31-4.03 (m, 1H), 3.65- 3.55 (m, 1H), 3.54-3.43 (m, 2H), 2.13-2.05 (m, 2H), 2.04- 1.96 (m, 2H), 1.70-1.62 (m, 2H), 1.55-1.35 (m, 6H), 1.27 (d, J = 8.0 Hz, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 400.53 [M + H]⁺. 44

UNC3200A ¹H NMR (400 MHz, CD3OD) δ 8.60 (s, 1H), 8.00 (br, 1H), 6.76 (s, 1H), 4.16-4.08 (m, 1H), 3.65-3.55 (m, 1H), 3.54- 3.43 (m, 2H), 2.12-2.04 (m, 2H), 2.04-1.95 (m, 2H), 1.70- 1.62 (m, 2H), 1.51 (s, 9H), 1.49-1.30 (m, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 414.56 [M + H]⁺. 45

UNC3190A ¹H NMR (400 MHz, CD3OD) δ 8.59 (s, 1H), 8.05 (s, 1H), 6.82 (s, 1H), 4.14-4.08 (m, 1H), 3.60-3.47 (m, 1H), 3.46- 3.39 (m, 4H), 2.14-1.95 (m, 4H), 1.75-1.62 (m, 4H), 1.55- 1.38 (m, 6H), 1.00 (dt, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 3H). MS m/z 400.53 [M + H]⁺. 46

UNC3193A ¹H NMR (400 MHz, CD3OD) δ 8.61 (s, 1H), 8.19 (br, 1H), 7.07 (s, 1H), 4.16-4.09 (m, 1H), 3.65-3.55 (m, 1H), 3.55- 3.45 (m, 2H), 2.15-2.05 (m, 2H), 2.05-1.97 (m, 2H), 1.72- 1.63 (m, 2H), 1.55-1.35 (m, 6H), 1.00 (t, J = 8.0 H,z, 3H), 0.97-0.93 (m, 2H), 0.72-0.67 (m, 2H). MS m/z 398.52 [M + H]⁺. 47

UNC3195A ¹H NMR (400 MHz, CD3OD) δ 8.61 (s, 1H), 8.03 (br, 1H), 6.80 (s, 1H), 4.55-4.43 (m, 1H), 4.16-4.08 (m, 1H), 3.65- 3.53 (m, 1H), 2.17-1.96 (m, 6H), 1.85-1.75 (m, 2H), 1.75- 1.55 (m, 6H), 1.54-1.33 (m, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 412.54 [M + H]⁺. 48

UNC3194A ¹H NMR (400 MHz, CD3OD) δ 8.62 (s, 1H), 8.01 (br, 1H), 6.77 (s, 1H), 4.16-4.00 (m, 2H), 3.65-3.53 (m, 1H), 3.53- 3.45 (m, 2H), 2.10-1.96 (m, 6H), 1.87-1.80 (m, 2H), 1.75- 1.62 (m, 3H), 1.53-1.25 (m, 11H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 440.60 [M + H]⁺. 49

UNC3199A ¹H NMR (400 MHz, CD3OD) δ 8.58 (s, 1H), 8.22 (br, 1H), 6.90 (s, 1H), 4.17-4.08 (m, 1H), 3.80-3.45 (m, 7H), 2.20- 1.98 (m, 8H), 1.71-1.63 (m, 2H), 1.56-1.35 (m, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 426.57 [M + H]⁺. 50

UNC3198A ¹H NMR (400 MHz, CD3OD) δ 8.64 (s, 1H), 8.03 (br, 1H), 7.23 (s, 1H), 4.18-4.08 (m, 1H), 4.05-3.87 (m, 4H), 3.60- 3.45 (m, 3H), 2.10-1.95 (m, 4H), 1.85-1.62 (m, 8H), 1.53- 1.30 (m, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 426.57 [M + H]⁺. 51

UNC3196A ¹H NMR (400 MHz, CD3OD) δ 8.60 (s, 1H), 8.28 (br, 1H), 7.15 (s, 1H), 4.16-4.09 (m, 1H), 3.85-3.75 (m, 8H), 3.67- 3.57 (m, 1H), 3.55-3.43 (m, 2H), 2.15-2.05 (m, 3H), 2.05- 1.97 (m, 2H), 1.71-1.62 (m, 2H), 1.55-1.35 (m, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 428.54 [M + H]⁺. 52

UNC3197A ¹H NMR (400 MHz, CD3OD) δ 8.72 (s, 1H), 8.36 (br, 1H), 7.37 (s, 1H), 4.10-4.10 (m, 1H), 3.75-3.57 (m, 4H), 3.55- 3.47 (m, 4H), 3.27-3.19 (m, 2H), 2.98 (s, 3H), 2.15-2.05 (m, 2H), 2.05-1.95 (m, 2H), 1.72-1.63 (m, 2H), 1.55-1.32 (m, 6H), 1.00 (d, J = 8.0 Hz, 3H). MS m/z 441.58 [M + H]⁺. 53

UNC3203A ¹H NMR (400 MHz, CD3OD) δ 8.65-8.61 (m, 1H), 8.43 (s, 1H), 8.08 (d, J = 8.0 Hz, 1H), 7.98-7.92 (m, 1H), 7.81-7.73 (m, 1H), 7.63 (d, J = 8.0 Hz, 1H), 7.61 (d, J = 8.0 Hz, 1H), 7.56-7.52 (m, 1H), 7.45-7.41 (m, 1H), 4.15-4.05 (m, 1H), 3.72-3.63 (m, 1H), 3.51 (s, 1H), 2.18 (d, J = 8.0 Hz, 1H), 2.04 (d, J = 8.0 Hz, 1H), 1.63- 1.35 (s, 4H), 1.00 (d, J = 8.0 Hz, 3H), 0.96-0.85 (m, 3H). MS m/z 386.46 [M + H]⁺. 54

UNC4223A ¹H NMR (400 MHz, CD₃OD) δ 8.37 (s, 1H), 8.00 (s, 1H), 4.74 (s, 2H), 4.20-4.10 (m, 1H), 3.71-3.62 (m, 1H), 3.50 (t, J = 6.8 Hz, 2H), 3.45-3.35 (m, 2H), 3.30 (quint, J = 1.6 Hz, 2H), 2.22-1.98 (m, 8H), 1.72-1.62 (m, 2H), 1.58-1.38 (m, 6H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 431.0 [M + H]⁺. 55

UNC4261A ¹H NMR (400 MHz, CD₃OD) δ 8.50 (s, 1H), 7.91 (s, 1H), 6.56 (s, 1H), 4.14-4.04 (m, 1H), 3.74-3.62 (m, 1H), 3.60- 3.53 (m, 1H), 3.53-3.45 (m, 2H), 2.10-1.93 (m, 6H), 1.80- 1.30 (m, 18H), 0.99 (t, J = 7.4 Hz, 3H); MS m/z 454.0 [M + H]⁺. 56

UNC4268A ¹H NMR (400 MHz, CD₃OD) δ 8.64 (s, 1H), 8.15 (s, 1H), 7.58 (d, J = 7.9 Hz, 2H), 7.37 (t, J = 5.8 Hz, 2H), 7.15 (t, J = 7.4 Hz, 1H), 7.10 (s, 1H), 4.15-4.05 (m, 1H), 3.67-3.60 (m, 1H), 3.55-3.40 (m, 2H), 2.15-1.95 (m, 4H), 1.65 (quint, J = 7.4 Hz, 2H), 1.55- 1.35 (m, 6H), 0.98 (t, J = 7.3 Hz, 3H); MS m/z 434.0 [M + H]⁺. 57

UNC4269A ¹H NMR (400 MHz, CD₃OD) δ 8.63 (s, 1H), 8.09 (s, 1H), 7.44 (d, J = 8.6 Hz, 2H), 7.00- 6.90 (m, 3H), 4.14-4.04 (m, 1H), 3.80 (s, 3H), 3.65-3.55 (m, 1H), 3.53-3.43 (m, 2H), 2.15-1.95 (m, 4H), 1.65 (quint, J = 7.4 Hz, 2H), 1.55- 1.32 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 464.0 [M + H]⁺. 58

UNC4270A ¹H NMR (400 MHz, CD₃OD) δ 8.74 (s, 1H), 8.09 (s, 1H), 7.32 (t, J = 8.2 Hz, 1H), 7.25 (s, 1H), 7.16-7.12 (m, 1H), 7.06 (s, 1H), 6.82 (dd, J = 8.3, 2.2 Hz, 1H), 4.15-4.05 (m, 1H), 3.81 (s, 3H), 3.65-3.55 (m, 1H), 3.53-3.43 (m, 2H), 2.15-1.95 (m, 4H), 1.65 (quint, J = 7.4 Hz, 2H), 1.56- 1.32 (m, 6H), 0.98 (t, J = 7.4 Hz, 3H); MS m/z 464.0 [M + H]⁺. 59

UNC4272A ¹H NMR (400 MHz, CD₃OD) δ 8.67 (s, 1H), 8.10 (s, 1H), 7.71 (d, J = 8.0 Hz, 1H), 7.32- 7.25 (m, 1H), 7.15-7.11 (m, 1H), 7.05-6.99 (m, 2H), 4.15- 4.05 (m, 1H), 3.88 (s, 3H), 3.65-3.55 (m, 1H), 3.53-3.43 (m, 2H), 2.15-1.95 (m, 4H), 1.65 (quint, J = 7.4 Hz, 2H), 1.55-1.33 (m, 6H), 0.98 (t, J = 7.3 Hz, 3H); MS m/z 464.0 [M + H]⁺. 60

UNC4322A ¹H NMR (400 MHz, CD₃OD) δ 8.82 (t, J = 2.2 Hz, 1H), 8.75 (s, 1H), 8.28 (s, 1H), 8.00- 7.89 (m, 2H), 7.56 (t, J = 8.2 Hz, 1H), 7.10 (s, 1H), 4.15- 4.05 (m, 1H), 3.75-3.63 (m, 1H), 3.55-3.45 (m, 2H), 2.25- 1.95 (m, 4H), 1.67 (quint, J = 7.4 Hz, 2H), 1.60-1.35 (m, 6H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 479.0 [M + H]⁺. 61

UNC4323A ¹H NMR (400 MHz, CD₃OD) δ 8.65 (s, 1H), 8.15 (s, 1H), 7.45-7.40 (m, 2H), 7.34-7.27 (m, 1H), 7.07 (d, J = 7.8 Hz, 1H), 7.02 (s, 1H), 4.16-4.06 (m, 1H), 3.68-3.63 (m, 1H), 3.55-3.45 (m, 2H), 2.92 (sept, J = 7.0 Hz, 1H), 2.20-1.95 (m, 4H), 1.66 (quint, J = 7.4 Hz, 2H), 1.56-1.36 (m, 6H), 1.27 (d, J = 7.0 Hz, 6H) 1.00 (t, J = 7.4 Hz, 3H); MS m/z 476.0 [M + H]⁺. 62

UNC4333A ¹H NMR (400 MHz, CD₃OD) δ 8.62 (s, 1H), 8.16 (s, 1H), 7.56-7.54 (m, 1H), 7.46-7.42 (m, 1H), 7.30 (t, J = 7.8 Hz, 1H), 7.23-7.19 (m, 1H), 7.00 (s, 1H), 4.16-4.07 (m, 1H), 3.70-3.62 (m, 1H), 3.54-3.44 (m, 2H), 2.20-1.95 (m, 4H), 1.66 (quint, J = 7.4 Hz, 2H), 1.55-1.40 (m, 6H), 1.34 (s, 9H), 1.00 (t, J = 7.4 Hz, 3H); MS m/z 490.0 [M + H]⁺. 63

UNC4353A ¹H NMR (400 MHz, CD₃OD) δ 8.65 (s, 1H), 8.21 (s, 1H), 7.87 (s, 1H), 7.65-7.58 (m, 3H), 7.48-7.32 (m, 5H), 7.04 (s, 1H), 4.15-4.05 (m, 1H), 3.75-3.55 (m, 1H), 3.55-3.40 (m, 2H), 2.20-1.95 (m, 4H), 1.66 (quint, J = 7.4 Hz, 2H), 1.57-1.37 (m, 6H), 1.00 (t, J = 7.3 Hz, 3H); MS m/z 510.0 [M + H]⁺. 64

UNC3664A ¹H NMR (400 MHz, CD₃OD) δ 8.84 (d, J = 2.0 Hz, 1H), 8.44 (s, 1H), 8.15 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.20-4.09 (m, 1H), 3.93 (s, 4H), 3.67-3.32 (m, 7H), 2.16 (d, J = 8.0 Hz, 2H), 2.02 (d, J = 8.0 Hz, 2H), 1.77-1.74 (m, 2H), 1.68-1.65 (m, 2H), 1.54-1.36 (m, 6H), 0.99 (t, J = 8.0 Hz, 3H). MS m/z 467.63 [M + H]⁺. 65

UNC3665A ¹H NMR (400 MHz, CD₃OD) δ 8.61 (d, J = 2.0 Hz, 1H), 8.23 (s, 1H), 7.95-7.87 (m, 2H), 8.01 (t, J = 4.0 Hz, 1H), 4.14 (s, 1H), 3.68-3.62 (m, 1H), 2.15 (s, 2H), 2.02-1.95 (m, 2H), 1.75-1.30 (m, 8H), 0.96 (t, J = 8.0 Hz, 3H), 0.89 (s, 4H). MS m/z 468.50 [M + H]⁺. 66

UNC3666A ¹H NMR (400 MHz, CD₃OD) δ 8.92 (d, J = 4.0 Hz, 1H), 8.47 (s, 1H), 8.21 (dd, J₁ = 4.0 Hz, J₂ = 8.0 Hz, 1H), 8.07 (d, J = 8.0 Hz, 1H), 4.20-4.12 (m, 1H), 4.10-3.81 (m, 4H), 3.78- 3.56 (m, 1H), 3.54-3.41 (m, 2H), 3.98-3.87 (m, 4H), 2.64 (br, 2H), 2.21-2.13 (m, 2H), 2.12-1.97 (m, 4H), 1.80-1.63 (m, 4H), 1.62-1.39 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 381.66 [M + H]⁺. 67

UNC3667A ¹H NMR (400 MHz, CD₃OD) δ 8.98 (d, J = 4.0 Hz, 1H), 8.48 (s, 1H), 8.28 (dd, J₁ = 4.0 Hz, J₂ = 8.0 Hz, 1H), 8.07 (d, J = 8.0 Hz, 1H), 4.20-4.12 (m, 1H), 4.02-3.85 (m, 4H), 3.70- 3.60 (m, 1H), 3.59-3.45 (m, 4H), 2.98-2.92 (m, 2H), 2.91- 2.80 (m, 2H), 2.36-2.27 (m, 2H), 2.21-2.14 (m, 2H), 2.06- 1.92 (m, 4H), 1.71-1.63 (m, 2H), 1.61-1.38 (m, 8H), 0.99 (t, J = 8.0 Hz, 3H). MS m/z 495.68 [M + H]⁺. 68

UNC3669A ¹H NMR (400 MHz, CD₃OD) δ 8.62 (s, 1H), 8.36 (s, 1H), 7.91 (m, 2H), 4.20-4.10 (m, 1H), 3.70-3.62 (m, 3H), 3.56- 3.40 (m, 4H), 3.26-3.10 (m, 4H), 2.82 (s, 3H), 2.56-2.47 (m, 2H), 2.22-2.13 (m, 2H), 2.13-1.95 (m, 4H), 1.75 (m, 2H), 1.60-1.38 (m, 5H), 1.36- 1.25 (m, 3H), 0.99 (t, J = 8.0 Hz, 3H). MS m/z 494.70 [M + H]⁺. 69

UNC4359A ¹H NMR (400 MHz, d- DMSO) δ 10.58 (s, 1H), 8.10 (d, J = 2.0 Hz, 1H), 7.94 (d, J = 2.0 Hz, 2H), 7.60 (d, J = 8.0 Hz, 1H), 7.18 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 3.49-3.42 (m, 2H), 2.00-1.91 (m, 2H), 1.86- 1.79 (m, 2H), 1.56-1.48 (m, 2H), 1.42-1.18 (m, 6H), 0.88 (t, J = 8.0 Hz, 3H). MS m/z 357.47 [M + H]⁺. 70

UNC3022A ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 4.9 Hz, 1H), 8.25 (s, 1H), 8.05 (d, J = 7.8 Hz, 1H), 7.93 (d, J = 8.2 Hz, 1H), 7.58-7.46 (m, 1H), 4.22- 3.98 (m, 1H), 3.68-3.53 (m, 1H), 3.48 (s, 2H), 2.13 (d, J = 11.7 Hz, 2H), 2.00 (d, J = 11.0 Hz, 2H), 1.75-1.62 (m, 2H), 1.43 (ddd, J = 16.6, 14.1, 9.7 Hz, 8H), 0.94 (t, J = 6.9 Hz, 3H). LC-MS (ESI+): t_(R) = 4.691 min, MS m/z 356.0 [M + 1]⁺; 71

UNC3051A ¹H NMR (400 MHz, CD₃OD) δ 8.77 (d, J = 5.1 Hz, 1H), 8.30 (td, J = 7.9, 1.5 Hz, 1H), 8.16 (s, 1H), 8.05 (d, J = 8.1 Hz, 1H), 7.75 (dd, J = 7.1, 5.9 Hz, 1H), 4.09 (dd, J = 12.4, 8.8 Hz, 1H), 3.71 (s, 2H), 3.59 (ddd, J = 9.8, 9.2, 4.1 Hz, 1H), 3.24 (s, 3H), 2.17-2.04 (m, 2H), 2.04-1.97 (m, 2H), 1.70 (dt, J = 15.2, 7.6 Hz, 2H), 1.61- 1.32 (m, 6H), 1.01 (t, J = 7.4 Hz, 3H). LC-MS (ESI+): t_(R) = 4.381 min, MS m/z 356.0 [M + 1]⁺. 72

UNC3053A ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J = 5.0 Hz, 1H), 8.28 (s, 1H), 8.09-7.92 (m, 1H), 7.89 (d, J = 8.2 Hz, 1H), 7.44 (dd, J = 7.0, 5.5 Hz, 1H), 4.09 (t, J = 10.3 Hz, 1H), 3.89 (s, 1H), 3.65 (tt, J = 8.4, 4.1 Hz, 1H), 2.15 (d, J = 11.2 Hz, 2H), 2.02 (d, J = 11.9 Hz, 4H), 1.94-1.78 (m, 2H), 1.69 (d, J = 12.5 Hz, 1H), 1.62-1.20 (m, 9H). LC-MS (ESI+): t_(R) = 4.495 min, MS m/z 368.0 [M + 1]⁺. 73

UNC3052A ¹H NMR (400 MHz, CD₃OD) δ 8.66 (d, J = 5.1 Hz, 1H), 8.21 (s, 1H), 8.12-8.01 (m, 1H), 7.96 (d, J = 8.1 Hz, 1H), 7.53 (dd, J = 7.4, 5.3 Hz, 1H), 4.08 (td, J = 10.2, 4.8 Hz, 1H), 3.79 (s, 4H), 3.66-3.58 (m, 1H), 2.13 (d, J = 11.1 Hz, 2H), 2.05-1.92 (m, 2H), 1.84- 1.69 (m, 6H), 1.56-1.36 (m, 4H). LC-MS (ESI+): t_(R) = 4.269 min, MS m/z 354.0 [M + 1]⁺.

Example 9 General Procedure for Table 9

A mixture of 2-pyridinyl trihydroxyborate lithium (1.32 g, 9 mmol, 3.0 eq.), copper bromide (85.8 mg, 0.6 mmol, 0.2 eq.) in a mixture of DMF and H₂O (4:1, 15 mL) was added potassium carbonate (1.24 g, 9 mmol, 3.0 eq.), 4-((5-bromo-2-chloropyrimidin-4-yl)amino)cyclohexan-1-ol (1.12 g, 3.0 mmol, 1.0 eq), and PdCl₂(dppf) (246 mg, 0.3 mmol, 0.1 eq.). The resulting mixture was heated at 120° C. in the open air for 30 min, then allowed to cool to room temperature. The insoluble material was removed by filtration through a short pad of celite, which was washed with DMF. The solvents were removed under the reduced pressure. The residue was filtered through a short pad of silica gel to remove the palladium black. The crude product was used without further purification.

A solution of crude 4-((2′-chloro-[4,5′-bipyrimidin]-4′-yl)amino)cyclohexanol (183 mg, 0.6 mmol) and 4-vinylaniline (86 mg, 0.72 mmol) in THF (1.5 mL) was added Pd(OAc)₂ (45 mg, 0.12 mmol), BINAP (75.0 mg, 0.12 mmol) and Cs₂CO₃ (470 mg, 0.72 mmol) in sequence. The resulting mixture was heated at 140° C. in the open air for 30 min, then allowed to cool to room temperature. The solvent was removed and the residue was purified by ISCO with dry loading to afford the desired compound (104 mg, 31%)(UNC3204A). ¹H NMR (400 MHz, CD3OD) δ 8.70-8.68 (m, 1H), 8.36 (s, 1H), 8.10 (dt, J₁=2.0 Hz, J₂=8.0 Hz, 1H), 7.99 (d, J=8.0 Hz, 1H), 7.59-7.52 (m, 5H), 7.76 (dd, 2.0 Hz, J₂=8.0 Hz, 1H), 5.81 (dd, J₁=2.0 Hz, J₂=20.0 Hz, 1H), 5.27 (dd, J₁=2.0 Hz, J₂=12.0 Hz, 1H), 4.15-4.05 (m, 1H), 3.69-3.60 (m, 1H), 2.20-2.10 (m, 2H), 2.06-1.96 (m, 2H), 1.60-1.58 (m, 2H), 1.50-1.35 (m, 2H). MS m/z 388.49 [M+H]⁺.

Table 9 describes compounds could be prepared following procedures described in Example 9, using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR  1

UNC3204A ¹H NMR (400 MHz, CD3OD) δ 8.70-8.68 (m, 1H), 8.36 (s, 1H), 8.10 (dt, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.99 (d, J = 8.0 Hz, 1H), 7.59-7.52 (m, 5H), 7.76 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 5.81 (dd, J₁ = 2.0 Hz, J₂ = 20.0 Hz, 1H), 5.27 (dd, J₁ = 2.0 Hz, J₂ = 12.0 Hz, 1H), 4.15-4.05 (m, 1H), 3.69-3.60 (m, 1H), 2.20-2.10 (m, 2H), 2.06-1.96 (m, 2H), 1.60-1.58 (m, 2H), 1.50-1.35 (m, 2H). MS m/z 388.49 [M + H]⁺.  2

UNC3223A ¹H NMR (400 MHz, CD3OD) δ 8.64 (dd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, 1H), 8.43 (s, 1H), 7.90- 7.98 (m, 3H), 7.47-7.36 (m, 4H), 4.20-4.06 (m, 1H), 3.82- 3.63 (m, 1H), 3.61 (s, 1H), 2.21-2.15 (m, 2H), 2.06-1.98 (m, 2H), 1.60-1.45 (m, 4H). MS m/z 386.47 [M + H]⁺.  3

UNC3206A ¹H NMR (400 MHz, CD3OD) δ 8.91 (s, 1H), 7.75 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.17 (d, J =8.0 Hz, 1H), 8.06 (dt, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.63 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.57-7.52 (m, 2H), 7.36 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 2H), 7.09 (s, 1H), 4.48-4.35 (m, 1H), 3.76- 3.60 (m, 1H), 2.30-2.22 (m, 2H), 2.10-2.02 (m, 2H), 1.70- 1.58 (m, 2H), 1.53-1.40 (m, 2H). MS m/z 386.46 [M + H]⁺.  4

UNC3207A ¹H NMR (400 MHz, d- DMSO) δ 11.33 (s, 1H), 10.92 (s, 1H), 8.72 (s, 1H), 8.62 (s, 1H), 8.22 (s, 1H), 8.06-7.78 (m, 3H), 7.66 (s, 1H), 7.51 (s, 1H), 7.44 (s, 1H), 5.69 (s, 1H), 3.99 (s, 1H), 3.13 (s, 1H), 2.11-1.80 (m, 4H), 1.60-1.11 (m, 4H). MS m/z 412.51 [M + H]⁺.  5

UNC3205A ¹H NMR (400 MHz, d- DMSO) δ 11.03 (d, J = 2.0 Hz, 1H), 10.52 (s, 1H), 8.61 (dt, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.56 (br, 1H), 8.07-7.92 (m, 4H), 7.76 (d, J = 8.0 Hz, 1H), 7.61-7.55 (m, 2H), 7.48-7.41 (m, 1H), 1.80-1.68 (m, 4H), 1.32-1.20 (m, 2H), 0.98-0.93 (m, 2H). MS m/z 412.51 [M + H]⁺.  6

 7

 8

UNC3224A ¹H NMR (400 MHz, d- DMSO) δ 8.70 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 2H), 8.56 (s, 1H), 8.43 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 2H), 8.11 (td, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.11 (dt, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.95 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 1H), 7.57 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 1H), 7.26 (td, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 2H), 4.28-4.20 (m, 1H), 3.72-3.65 (m, 1H), 2.22- 2.14 (m, 2H), 2.07-2.00 (m, 2H), 1.60-1.40 (m, 4H). MS m/z 363.44 [M + H]⁺.  9

UNC3209A ¹H NMR (400 MHz, CD3OD) δ 9.35 (d, J = 2.0 Hz, 1H), 8.88 (d, J = 2.0 Hz, 1H), 8.76- 8.73 (m, 2H), 8.56 (s, 1H), 8.23-8.13 (s, 2H), 8.11 (d, J = 8.0 Hz, 1H), 7.68-7.65 (m, 1H), 4.13-4.07 (m, 1H), 3.70- 3.64 (m, 1H), 2.16-2.12 (m, 2H), 2.04-2.00 (m, 2 H), 1.58- 1.44 (m, 4 H). MS m/z 412.51 [M + H]⁺. 10

UNC3208A ¹H NMR (400 MHz, d- DMSO) δ 11.12 (s, 1H), 10.27 (d, J = 8.0 Hz, 1H), 8.78 (s, 1H), 8.62 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 2H), 8.56 (d, J = 4.0 Hz, 2H), 8.23 (d, J = 8.0 Hz, 2H), 8.07 (d, J = 8.0 Hz, 1H), 7.93 (td, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.38 (ddd, J₁ = 2.0 Hz, J₂ = 4.0 Hz, J₃ = 8.0 Hz, 1H), 3.98 (s, 1H), 2.11-2.00 (m, 2H), 1.90-1.80 (m, 2H), 1.45-1.32 (m, 4H). MS m/z 412.51 [M + H]⁺. 11

12

UNC4240A ¹H NMR (400 MHz, CD₃OD) δ 8.79 (s, 1H), 8.44 (m, 1H), 8.13-8.05 (m, 2H), 7.43 (d, J = 8.0 Hz, 2H), 7.03 (d, J = 8.0 Hz, 2H), 4.51 (s, 2H), 4.09- 4.08 (m, 1H), 3.86 (s, 1H), 3.64-3.48 (m, 3H), 3.26-3.21 (m, 3H), 2.23-1.99 (m, 9H), 1.57-1.39 (m, 4H); MS m/z 475.30 [M + 1]⁺. 13

UNC4241A ¹H NMR (400 MHz, CD₃OD) δ 8.79 (s, 1H), 8.50 (m, 1H), 8.14-8.07 (m, 2H), 7.58-7.55 (m. 2H), 7.25-7.20 (m, 2H), 4.52 (s, 2H), 4.06-4.03 (m, 1H), 3.65-3.47 (m, 3H), 3.21- 3.28 (m, 2H), 2.16-1.99 (m, 8H), 1.54-1.38 (m, 4H); MS m/z 463.30 [M + 1]⁺. 14

UNC4242A ¹H NMR (400 MHz, CD₃OD) δ 8.74 (s, 1H), 8.49 (s, 1H), 8.05-8.02 (m, 2H), 7.48 (d, J = 8.0 Hz, 2H), 7.24 (d, J = 8.0 Hz, 2H), 4.49 (s, 2H), 4.11- 4.08 (m, 1H), 3.66-3.48 (m, 3H), 3.27-3.24 (m, 2H), 2.37 (s, 3H), 2.22-1.99 (m, 8H), 1.52-1.43 (m, 4H); MS m/z 459.30 [M + 1]⁺. 15

UNC4243A ¹H NMR (400 MHz, CD₃OD) δ 8.79 (s, 1H), 8.60 (s, 1H), 8.11-8.13 (m, 2H), 7.86 (d, J = 8.0 Hz, 2H), 7.75 (d, J = 8.0 Hz, 2H), 4.52 (s, 2H), 4.15- 4.09 (m, 1H), 3.69-3.55 (m, 3H), 3.22-3.29 (m, 2H), 2.27- 2.01 (m, 8H), 1.57-1.44 (m, 4H); MS m/z 513.30 [M + 1]⁺. 16

UNC4244A ¹H NMR (400 MHz, CD₃OD) δ 8.79 (s, 1H), 8.56 (s, 1H), 8.10-8.08 (m, 2H), 7.77-7.75 (m, 1H), 7.39-7.29 (m, 3H), 4.52 (s, 2H), 4.01-3.94 (m, 1H), 3.64-3.48 (m, 3H), 3.21- 3.26 (m, 2H), 2.23-1.98 (m, 8H), 1.52-1.32 (m, 4H); MS m/z 463.30 [M + 1]⁺. 17

UNC4247A ¹H NMR (400 MHz, CD₃OD) δ 8.78 (s, 1H), 8.53 (s, 1H), 8.14-8.07 (m, 2H), 7.61-7.58 (m, 1H), 7.45-7.42 (m, 1H), 7.30-7.27 (m, 1H), 7.03-6.99 (m, 1H), 4.50 (s, 2H), 4.07- 4.11 (m, 1H), 3.66-3.53 (m, 2H), 3.23-3.19 (m, 3H), 2.21- 1.97 (m, 8H), 1.64-1.39 (m, 4H); MS m/z 463.30 [M + 1]⁺. 18

UNC4372A ¹H NMR (400 MHz, CD₃OD) δ 8.81 (d, J = 1.6 Hz, 1H), 8.62 (s, 1H), 8.20-8.10 (m, 2H), 7.87-7.81 (m, 4H), 4.52 (s, 2H), 4.15-4.08 (m, 1H), 3.69- 3.55 (m, 3H), 2.21-1.98 (m, 9H), 1.62-1.41 (m, 4H); MS m/z 470.30 [M + 1]⁺. 19

UNC4373A ¹H NMR (400 MHz, CD₃OD) δ 8.78 (s, 1H), 8.53 (s, 1H), 8.16-8.07 (m, 2H), 7.59 (d, J = 8.8 Hz, 2H), 7.46 (d, J = 8.8 Hz, 2H), 4.51 (s, 2H), 4.08- 4.04 (m, 1H), 3.66-3.56 (m, 3H), 2.22-2.02 (m, 8H), 1.55- 1.41 (m, 4H); MS m/z 479.30 [M + 1]⁺. 20

UNC4377A ¹H NMR (400 MHz, CD₃OD) δ 8.54 (s, 1H), 8.13 (s, 1H), 8.16-8.07 (m, 2H), 7.61-7.54 (m, 4H), 4.51 (s, 2H), 4.10- 4.05 (m, 1H), 3.66-3.52 (m, 3H), 2.18-1.98 (m, 8H), 1.58- 1.38 (m, 4H); MS m/z 523.20 [M + 1]⁺. 21

UNC4397A ¹H NMR (400 MHz, CD₃OD) δ 8.55 (s, 1H), 8.43 (s, 1H), 7.96-7.84 (m, 2H), 7.59-7.56 (m. 2H), 7.23-7.19 (m, 2H), 6.57 (s, 1H), 4.06-4.01 (m, 1H), 3.75-3.52 (m, 6H), 3.16- 3.03 (m, 3H), 2.90-2.64 (m, 3H), 2.15-2.12 (m, 2H), 2.04- 1.96 (m, 2H), 1.57-1.47 (m, 2H), 1.39 (m, 8H); MS m/z 517.30 [M + 1]⁺. 22

UNC4398A ¹H NMR (400 MHz, CD₃OD) δ 8.55 (s, 1H), 8.42 (s, 1H), 7.97-7.86 (m, 2H), 7.59-7.56 (m. 2H), 7.24-7.19 (m, 2H), 4.06-4.00 (m, 1H), 3.75-3.48 (m, 6H), 3.16-2.73 (m, 7H), 2.13-1.91 (m, 6H), 1.59-1.34 (m, 5H); MS m/z 419.35 [M + 1]⁺.

Example 10 General Procedure for Table 10

A solution of 6-(2-(butylamino)-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)nicotinaldehyde (370 mg, 1 mmol) in MeOH (5.0 mL) was added NaBH₄ (76 mg, 2.0 mmol) at room temperature. The reaction mixture was stirred at room temperature for 30 min, quenched with brine and extracted with DCM (20 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated. The residue was used in the next step without further purification.

A solution of crude trans-4-((2-(butylamino)-5-(5-(hydroxymethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (372 mg, 1 mmol) in DCM (10 mL) was added MsCl (138 mg, 1.2 mmol) and DIPEA (194 mg, 1.5 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 30 min, quenched with brine and extracted with DCM (20 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated. A solution of the residue in isopropyl alcohol (6.0 mL) was added tert-butyl 2,6-dimethylpiperazine-1-carboxylate (258 mg, 1.2 mmol) and DIPEA (194 mg, 1.5 mmol). The reaction mixture was heated at 110° C. for 24 hours. After cooling down to room temperature, the reaction was diluted by DCM (20 mL). The organic layer was dried (MgSO₄) and concentrated. The residue was then dissolved in 3 N HCl in methanol (6.0 mL) and stirred overnight. The solvent was the removed and the residue was purified using HPLC to afford the desired compound (49 mg, 8%) (UNC4105A). ¹H NMR (400 MHz, CD₃OD) δ 8.86 (d, J=4.0 Hz, 1H), 8.43 (s, 1H), 8.25 (dd, J=2.0 Hz, J=8.0 Hz, 1H), 8.02 (d, J=8.0 Hz, 1H), 4.55 (s, 2H), 4.21-4.12 (m, 1H), 3.93-3.82 (m, 1H), 3.72-3.63 (m, 3H), 3.55-3.45 (m, 2H), 3.28-3.24 (m, 2H), 2.22-2.13 (m, 2H), 2.09-1.96 (m, 2H), 1.74-1.64 (m, 2H), 1.60-1.40 (m, 12H), 1.00 (t, J=8.0 Hz, 3H). MS m/z 468.66 [M+H]⁺.

Table 10 describes compounds could be prepared following procedures described in Example 10, using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR  1

UNC4105A ¹H NMR (400 MHz, CD₃OD) δ 8.86 (d, J = 4.0 Hz, 1H), 8.43 (s, 1H), 8.25 (dd, J = 2.0 Hz, J = 8.0 Hz, 1H), 8.02 (d, J = 8.0 Hz, 1H), 4.55 (s, 2H), 4.21- 4.12 (m, 1H), 3.93-3.82 (m, 1H), 3.72-3.63 (m, 3H), 3.55- 3.45 (m, 2H), 3.28-3.24 (m, 2H), 2.22-2.13 (m, 2H), 2.09- 1.96 (m, 2H), 1.74-1.64 (m, 2H), 1.60-1.40 (m, 12H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 468.66 [M + H]⁺.  2

UNC4106A ¹H NMR (400 MHz, CD₃OD) δ 8.82 (d, J = 4.0 Hz, 1H), 8.42 (s, 1H), 8.20 (dd, J = 2.0 Hz, J = 8.0 Hz, 1H), 8.00 (d, J = 8.0 Hz, 1H), 4.44 (s, 2H), 4.21- 4.12 (m, 1H), 3.88-3.82 (m, 1H), 3.21-3.10 (m, 1H), 2.22- 2.13 (m, 2H), 2.05-1.98 (m, 2H), 1.72-1.64 (m, 2H), 1.60- 1.38 (m, 9H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 454.64 [M + H]⁺.  3

UNC4109A ¹H NMR (400 MHz, CD₃OD) δ 8.85 (d, J = 4.0 Hz, 1H), 8.43 (s, 1H), 8.23 (dd, J = 2.0 Hz, J = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.96 (d, J = 12.0 Hz, 1H), 4.30 (d, J = 12.0 Hz, 1H), 3.90-3.76 (m, 2H), 3.75-3.64 (m, 2H), 3.60-3.45 (m, 3H), 3.45-3.37 (m, 1H), 3.28-3.19 (m, 1H), 2.22-2.12 (m, 2H), 2.07-1.96 (m, 2H), 1.75-1.61 (m, 5H), 1.60-1.39 (m, 6H), 1.34 (t, J = 8.0 Hz, 3H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 468.66 [M + H]⁺.  4

UNC4110A ¹H NMR (400 MHz, CD₃OD) δ 8.85 (s, 1H), 8.42 (s, 1H), 8.25 (d, J = 8.0 Hz, 1H), 8.00 (d, J = 8.0 Hz, 1H), 4.21-4.11 (m, 1H), 3.75-3.43 (m, 11H), 2.21-2.13 (m, 2H), 2.06-1.98 (m, 2H), 1.76 (s, 6H), 1.73- 1.63 (m, 2H), 1.62-1.38 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 468.66 [M + H]⁺.  5

UNC4111A ¹H NMR (400 MHz, CD₃OD) δ 8.87 (d, J = 2.0 Hz, 1H), 8.44 (s, 1H), 8.27 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.02 (d, J = 8.0 Hz, 1H), 4.97 (d, J = 12.0 Hz, 1H), 4.38 (d, J = 12.0 Hz, 1H), 4.21-4.12 (m, 1H), 3.98- 3.87 (m, 1H), 3.75-3.60 (m, 4H), 3.60-3.55 (m, 1H), 3.55- 3.45 (m, 2H), 3.76-3.43 (m, 9H), 2.21-2.12 (m, 2H), 2.06- 1.98 (m, 2H), 1.75-1.63 (m, 5H), 1.62-1.39 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 454.64 [M + H]⁺.  6

UNC4112A ¹H NMR (400 MHz, CD₃OD) δ 8.92 (s, 1H), 8.44 (s, 1H), 8.22 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.02 (d, J = 8.0 Hz, 1H), 4.75 (d, J = 12.0 Hz, 1H), 4.66 (s, 2H), 4.59 (d, J = 12.0 Hz, 1H), 4.22-4.09 (m, 2H), 3.86 (d, J = 12.0 Hz, 1H), 3.75-3.64 (m, 2H), 3.62-3.55 (m, 1H), 3.55-3.45 (m, 2H), 2.90-2.75 (m, 1H), 2.33 (d, J = 16.0 Hz, 1H), 2.21-2.12 (m, 2H), 2.06-1.98 (m, 2H), 1.72- 1.63 (m, 2H), 1.62-1.38 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 452.62 [M + H]⁺.  7

UNC4113A ¹H NMR (400 MHz, CD₃OD) δ 8.83 (d, J = 2.0 Hz, 1H), 8.43 (s, 1H), 8.22 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 8.00 (d, J = 8.0 Hz, 1H), 4.49 (s, 2H), 4.20- 4.12 (m, 1H), 3.89-3.78 (m, 1H), 3.72-3.60 (m, 4H), 3.60- 3.55 (m, 1H), 3.55-3.45 (m, 2H), 3.43-3.33 (1H), 3.22 (t, J = 12.0 Hz, 1H), 2.21-2.12 (m, 2H), 2.06-1.98 (m, 2H), 1.72- 1.63 (m, 2H), 1.62-1.38 (m, 9H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 454.64 [M + H]⁺.  8

UNC4160A ¹H NMR (400 MHz, CD₃OD) δ 8.73 (d, J = 2.0 Hz, 1H), 8.40 (s, 1H), 8.08 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.98 (d, J = 8.0 Hz, 1H), 4.28 (s, 2H), 4.19- 4.08 (m, 1H), 3.70-3.63 (m, 1H), 3.55-3.40 (m, 2H), 2.20- 2.12 (m, 2H), 2.06-1.98 (m, 2H), 1.69-1.61 (m, 3H), 1.60- 1.38 (m, 14H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 427.61 [M + H]⁺.  9

UNC4166A 1H NMR (400 MHz, CD3OD) δ 8.69 (s, 1H), 8.40 (s, 1H), 8.03 (d, J = 8.0 Hz, 1H), 7.97 (d, J = 8.0 Hz, 1H), 4.28 (s, 2H), 4.18-4.09 (m, 1H), 3.70- 3.61 (m, 1H), 3.53-3.42 (m, 2H), 2.24 (s, 3H), 2.20-2.13 (m, 2H), 2.05-1.95 (m, 8H), 1.83 (d, J = 12.0 Hz, 3H), 1.75 (d, J = 12.0 Hz, 3H), 1.70-1.60 (m, 2H), 1.55-1.37 (m, 6H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 505.72 [M + H]+. 10

UNC4167A 1H NMR (400 MHz, CD3OD) δ 8.78 (s, 1H), 8.43 (s, 1H), 8.14 (d, J = 8.0 Hz, 1H), 8.01 (d, J = 8.0 Hz, 1H), 4.36 (s, 2H), 4.20-4.10 (m, 1H), 4.08 (s, 1H), 3.70-3.60 (m, 1H), 3.52-3.40 (m, 2H), 2.39-2.31 (m, 2H), 2.20-2.12 (m, 2H), 2.10-1.96 (m, 4H), 1.96-1.86 (m, 2H), 1.86-1.78 (m, 2H), 1.70-1.60 (m, 2H). 1.59-1.35 (m, 6H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 451.63 [M + H]+. 11

UNC4168A 1H NMR (400 MHz, CD3OD) δ 8.75 (s, 1H), 8.44 (s, 1H), 8.09 (d, J = 8.0 Hz, 1H), 8.02 (d, J = 8.0 Hz, 1H), 4.39 (s, 2H), 4.20-4.10 (m, 1H), 3.70- 3.61 (m, 1H), 3.56-3.40 (m, 2H), 2.22 (s, 1H), 2.20-2.12 (m, 2H), 2.14-1.95 (m, 2H), 1.70-1.60 (m, 2H), 1.56-1.38 (m, 6H), 1.07 (s, 6H), 0.98 (t, J = 8.0 Hz, 3H), 0.95 (s, 6H). MS m/z 467.67 [M + H]+. 12

UNC4196A 1H NMR (400 MHz, CD3OD) δ 8.55 (s, 1H), 8.29 (s, 1H), 8.87 (d, J = 8.0 Hz, 1H), 8.84 (d, J = 8.0 Hz, 1H), 4.58 (s, 2H), 4.20-4.11 (m, 1H), 3.75- 3.70 (m, 1H), 3.69-3.59 (m, 1H), 3.51-3.44 (m, 2H), 2.22- 2.15 (m, 2H), 2.15-2.07 (m, 2H), 1.92-1.73 (m, 4H), 1.61- 1.38 (m, 4H), 1.22 (d, J = 4.0 Hz, 6H), 0.98 (t, J = 8.0 Hz, 3H). MS m/z 414.57 [M + H]+. 13

UNC4169A 1H NMR (400 MHz, CD3OD) δ 8.80 (s, 1H), 8.45 (s, 1H), 8.19 (d, J = 8.0 Hz, 1H), 8.04 (d, J = 8.0 Hz, 1H), 4.30 (s, 2H), 4.22-4.13 (m, 1H), 3.96 (s, 2H), 3.72-3.63 (m, 1H), 3.55-3.46 (m, 1H), 2.49-2.42 (m, 2H), 2.22-2.15 (m, 2H), 2.15-2.07 (m, 2H), 2.07-1.96 (m, 4H), 1.90-1.74 (m, 3H), 1.72-1.60 (m, 3H). 1.60-1.39 (m, 6H), 1.01 (t, J = 8.0 Hz, 3H). MS m/z 465.66 [M + H]+.

Example 11 General Procedure for Table 11

A solution of 4-((2-(butylamino)-5-(5-chloropyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol (188 mg, 0.50 mmol) in DMF (5.0 mL) was added TBSCl (113 mg, 0.75 mmol) and imidazole (103 mg, 1.55 mmol). The reaction mixture was stirred at room temperature overnight, quenched with brine (10 mL), and extracted with DCM (20 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated. The residue was used in the next step without further purification.

A solution of N²-butyl-N⁴-(4-((tert-butyldimethylsilyl)oxy)cyclohexyl)-5-(5-chloropyridin-2-yl)pyrimidine-2,4-diamine (188 mg, 0.50 mmol) in CH₃CN (2.0 mL) was added cesium carbonate (326 mg, 1.0 mmol), Xphos (36 mg, 0.075 mmol), and PdCl₂(CH₃CN)₂ (6.6 mg, 0.025 mmol) in sequence. The mixture was stirred for 5 min before the addition of prop-2-yn-1-ol (58 mg, 1.00 mmol). The reaction mixture was then heated at 90° C. overnight, quenched with brine and extracted with DCM (20 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated. A solution of the residue in MeOH (5.0 mL) was added 10% palladium on carbon (20 mg, 10% w/w). The reaction mixture was stirred under H₂ atmosphere (balloon) for 24 hours and passed through a plug of silica. The solvent was removed under the reduced pressure to afford the crude 34642-(butylamino)-4-(4-((tert-butyldimethylsilyl)oxy)cyclohexyl)amino)pyrimidin-5-yl)pyrid-in-3-yl)propan-1-ol which was used in the next step without further purification.

A solution of crude 3-(6-(2-(butylamino)-4-(4-((tert-butyldimethylsilyl)oxy)cyclohexyl)amino)pyrimidin-5-yl)pyrid-in-3-yl)propan-1-ol (257 mg, 0.50 mmol) in DCM (6.0 mL) was added MsCl (59 uL, 0.75 mmol). The reaction mixture was stirred at 0° C. for 1 hour, then was added DIPEA (0.27 mL, 1.5 mmol). The reaction mixture was stirred at 0° C. for another hour, quenched by water, and extracted with DCM (20 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated to provide the crude product which was dissolved in CH₃CN (1.5 mL) and was treated with DIPEA (0.27 mL, 1.5 mmol) and pyrrolidine (108 mg, 1.5 mmol). The reaction mixture was heated at 110° C. in sealed tube overnight, quenched with brine (10 mL), and extracted with DCM (20 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated. The residue was dissolved in 3 N HCl in MeOH (5.0 mL) and was stirred overnight. Then, the solvent was removed under the reduced pressure and the residue was purified using HPLC to afford the desired compound (84 mg, 30%) (UNC4220A). ¹H NMR (400 MHz, CD₃OD) δ 8.56 (d, J=4.0 Hz, 1H), 8.29 (s, 1H), 7.93 (d, J=8.0 Hz, 1H), 7.87 (d, J=8.0 Hz, 1H), 4.18-4.10 (m, 1H), 3.70-3.62 (m, 3H), 3.54-3.43 (m, 2H), 3.28-3.18 (m, 2H), 3.13-3.03 (m, 2H), 2.86-2.80 (m, 2H), 2.21-1.96 (m, 10H), 1.71-1.64 (m, 2H), 1.58-1.38 (m, 6H), 1.00 (t, J=8.0 Hz, 3H). MS m/z 453.65 [M+H]⁺.

Table 11 describes compounds could be prepared following procedures described in Example 11 using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

UNC4220A ¹H NMR (400 MHz, CD₃OD) δ 8.56 (d, J = 4.0 Hz, 1H), 8.29 (s, 1H), 7.93 (d, J = 8.0 Hz, 1H), 7.87 (d, J = 8.0 Hz, 1H), 4.18-4.10 (m, 1H), 3.70-3.62 (m, 3H), 3.54-3.43 (m, 2H), 3.28-3.18 (m, 2H), 3.13-3.03 (m, 2H), 2.86-2.80 (m, 2H), 2.21-1.96 (m, 10H), 1.71-1.64 (m, 2H), 1.58-1.38 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 453.65 [M + H]⁺. 2

UNC4221A ¹H NMR (400 MHz, CD₃OD) δ 8.60 (d, J = 4.0 Hz, 1H), 8.33 (s, 1H), 7.92 (d, J = 8.0 Hz, 1H), 7.89 (d, J = 8.0 Hz, 1H), 4.20-4.10 (m, 1H), 3.76-3.62 (m, 3H), 3.55-3.43 (m, 4H), 3.22-3.12 (m, 4H), 2.25-2.11 (m, 4H), 2.10-1.96 (m, 2H), 1.71-1.64 (m, 2H), 1.58-1.39 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 439.62 [M + H]⁺. 3

UNC4279A 1H NMR (400 MHz, CD3OD) δ 8.70 (d, J = 4.0 Hz, 1H), 8.29 (s, 1H), 8.09 (d, J = 8.0 Hz, 1H), 7.94 (d, J = 8.0 Hz, 1H), 4.20-4.10 (m, 1H), 4.05-3.55 (m, 12H), 3.55-3.40 (m, 3H), 3.01 (s, 3H), 2.50-2.32 (m, 2H), 2.21-2.09 (m, 2H), 2.06- 1.96 (m, 2H), 1.72-1.63 (m, 2H), 1.60-1.38 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 482.69 [M + H]+. 4

UNC4281A 1H NMR (400 MHz, CD3OD) δ 8.63 (d, J = 4.0 Hz, 1H), 8.32 (s, 1H), 7.99 (d, J = 8.0 Hz, 1H), 7.92 (d, J = 8.0 Hz, 1H), 4.20-4.10 (m, 1H), 3.71-3.62 (m, 1H), 3.55-3.43 (m, 4H), 3.22-3.15 (m, 2H), 2.98 (s, 6H), 2.23-2.12 (m, 2H), 2.06- 1.96 (m, 2H), 1.72-1.63 (m, 2H), 1.60-1.38 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 413.58 [M + H]+.

Example 12 General Procedure for Table 12

A solution of (2-chloro-4-((4-hydroxycyclohexyl)amino)pyrimidin-5-yl)boronic acid (272 mg, 1.0 mmol) and 2-bromo-4-chloro-5-(pyrrolidin-1-ylmethyl)pyridine (414 mg, 1.5 mmol) in a mixture of dioxane (13 mL) and water (2.0 mL) was added Pd₂(dba)₃ (92 mg, 0.1 mmol) and PCy₃ (85 mg, 0.3 mmol). The reaction mixture was heated at 120° C. for 20 min. After cooling to room temperature, ethyl acetate (20 mL) was added and the mixture was washed with brine. The combined organic layer was dried (MgSO₄) and concentrated. The residue was passed through a short pad of celite to afford the crude product.

A solution of the crude product in isopropyl alcohol (10 mL) was added n-butylamine (1.0 mL) at room temperature. The reaction mixture was heated up at 90° C. overnight, quenched with brine (10 mL), and extracted with DCM (20 mL). The combined organic layer were was dried (MgSO₄) and concentrated. The residue was used in the next step without further purification.

The residue from last step was dissolved in a 4.4 N solution of CH₃ONa in MeOH (1.0 mL) and was added Pd(dppf)Cl₂ (41 mg, 0.05 mmol) and CuBr (14 mg, 0.1 mmol) at room temperature. The reaction mixture was heated at 110° C. for 30 min under microwave irradiation, quenched with brine (10 mL) at room temperature and extracted with ethyl acetate (20 mL) The combined organic layer was dried (MgSO₄) and concentrated. The residue was purified using ISCO to afford the desired product trans-4-((2-(butylamino)-5-(4-methoxy-5-(pyrrolidin-1-ylmethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (UNC4231A) (50 mg, 11%). ¹H NMR (400 MHz, CD₃OD) δ 8.56 (s, 1H), 8.48 (s, 1H), 7.60 (s, 1H), 4.45 (s, 2H), 4.13 (s, 3H), 3.70-3.45 (m, 7H), 2.25-2.10 (m, 2H), 2.09-1.96 (m, 2H), 1.68-1.64 (m, 2H), 1.55-1.47 (m, 6H), 0.99 (t, J=8.0 Hz, 3H). LC-MS (ESI+): t_(R)=3.805 min, MS m/z 455.0 [M+1]⁺.

Table 12 describes compounds could be prepared following procedures described in Example 12, using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

UNC4222A ¹H NMR (400 MHz, CD₃OD) δ 8.92 (s, 1H), 8.51 (s, 1H), 8.20 (s, 1H), 4.69 (s, 2H), 4.21-4.10 (m, 1H), 3.75-3.65 (m, 2H), 3.55-3.45 (m, 1H), 3.33-3.25 (m, 4H), 2.30-1.97 (m, 7H), 1.73-1.64 (m, 2H), 1.64-1.35 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 460.04 [M + H]⁺. 2

UNC4230A ¹H NMR (400 MHz, CD₃OD) δ 8.48 (s, 1H), 8.07 (s, 1H), 7.10 (s, 1H), 4.40 (s, 2H), 4.20-4.17 (m, 1H), 3.68-3.53 (m, 4H), 3.53-3.42 (m, 2H), 3.23-3.26 (m, 1H), 2.30-2.10 (m, 2H), 2.10-1.95 (m, 6H), 1.70-1.62 (m, 2H), 1.52-1.34 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 441.59 [M + H]⁺.

Example 13 General Procedure for Table 13

A mixture of SPhos (165 mg, 0.2 mol %), Pd(OAc)₂ (45 mg, 0.4 mmol), K₃PO₄ (850 mg, 4.0 mmol, 2.0 equiv), 4-((2-(butylamino)-5-(5-chloropyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol (752 mg, 2.0 mmol, 1 equiv, this compound could be prepared by procedure D in table 5), tert-butyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate (776 mg, 2.4 mmol, 2.0 equiv), CH₃CN (30 mL) and water (20 mL) in a 50 mL flask was stirred under Ar atmosphere at 90° C. overnight. The resulting mixture was passed through a pad of Celite and the pad was washed several times with EtOAc. The filtrate was washed with brine, dried (Na₂SO₄), and concentrated. The crude material was purified using ISCO to provide the desired product tert-butyl 4-((6-(2-(butylamino)-4-((4-hydroxycyclohexyl)amino)pyrimidin-5-yl)pyridin-3-yl)methylene) piperidine-1-carboxylate. A solution of crude tert-butyl 4-((6-(2-(butylamino)-4-((4-hydroxycyclohexyl)amino)pyrimidin-5-yl)pyridin-3-yl)methylene)piperidine-1-carboxylate (536 mg, 1 mmol) in MeOH (30 mL) was subjected to H-Cube at 80° C. and 100 bar. The solvent was removed and the crude product was treated with a 3.0 N HCl solution in MeOH (6.0 mL) overnight. The solvent was removed and the residue was purified using HPLC to afford pure the desired product trans-4-((2-(butylamino)-5-(5-(piperidin-4-ylmethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (202 mg, 37%) (UNC4335A). ¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.28 (s, 1H), 7.89 (s, 2H), 4.20-4.10 (m, 1H), 3.69-3.60 (m, 1H), 3.55-3.42 (m, 2H), 3.42-3.35 (m, 2H), 3.01-2.92 (m, 2H), 2.73 (d, J=8.0 Hz, 2H), 2.20-2.12 (m, 2H), 2.06-1.94 (m, 3H), 1.93-1.86 (m, 2H), 1.72-1.63 (m, 2H), 1.58-1.39 (m, 8H), 1.00 (t, J=8.0 Hz, 3H). MS m/z 439.62 [M+H]⁺.

A solution of trans-4-((2-(butylamino)-5-(5-(piperidin-4-ylmethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (44 mg, 0.1 mmol) in isopropyl alcohol (1.0 mL) was added DIPEA (26 mg, 0.2 mmol) and isopropyl iodide (51 mg, 0.6 mmol). The reaction mixture was heated at 110° C. overnight. The resulting mixture was filtered through a pad of Celite and the pad was washed several times with EtOAc. The filtrate was washed with brine, dried (Na₂SO₄), and concentrated. The residue was purified using ISCO and then HPLC to provide the desired product trans-4-((2-(butylamino)-5-(5-((1-isopropylpiperidin-4-yl)methyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (25 mg, 42%) (UNC4339A). ¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.28 (s, 1H), 7.90 (s, 2H), 4.19-4.10 (m, 1H), 3.70-3.61 (m, 1H), 3.55-3.42 (m, 4H), 3.00 (t, J=12.0 Hz, 2H), 3.74 (d, J=8.0 Hz, 2H), 2.20-2.12 (m, 2H), 2.05-1.92 (m, 5H), 1.71-1.41 (m, 10H), 1.33 (d, J=8.0 Hz, 6H), 1.00 (t, J=8.0 Hz, 3H). MS m/z 481.70 [M+H]⁺.

Table 13 describes compounds could be prepared following procedures described in Example 13, using appropriate reagents.

Physical Data Mer M/S m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

UNC4335A ¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.28 (s, 1H), 7.89 (s, 2H), 4.20-4.10 (m, 1H), 3.69-3.60 (m, 1H), 3.55- 3.42 (m, 2H), 3.42-3.35 (m, 2H), 3.01-2.92 (m, 2H), 2.73 (d, J = 8.0 Hz, 2H), 2.20-2.12 (m, 2H), 2.06-1.94 (m, 3H), 1.93-1.86 (m, 2H), 1.72-1.63 (m, 2H), 1.58-1.39 (m, 8H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 439.62 [M + H]⁺. 2

UNC4336A ¹H NMR (400 MHz, CD₃OD) δ 8.53 (d, J = 4.0 Hz, 1H), 8.34 (s, 1H), 7.90 (d, J = 8.0 Hz, 1H), 7.84 (dd, J₁ = 4.0 Hz, J₂= 8.0 Hz, 1H), 6.56 (s, 1H), 4.20-4.11 (m, 1H), 3.72-3.63 (m, 1H), 3.55-3.42 (m, 2H), 3.27-3.23 (m, 2H), 2.80-2.74 (m, 2H), 2.74-2.68 (m, 2H), 2.22-2.12 (m, 2H), 2.08-1.93 (m, 2H), 1.72-1.63 (m, 2H), 1.61-1.39 (m, 6H), 1.01 (t, J = 8.0 Hz, 3H). MS m/z 437.60 [M + H]⁺. 3

UNC4338A ¹H NMR (400 MHz, CD₃OD) δ 8.54 (s, 1H), 8.33 (s, 1H), 7.92 (d, J = 8.0 Hz, 1H), 7.87 (d, J₁ = 8.0 Hz, 1H), 6.59 (s, 1H), 4.23-4.11 (m, 1H), 3.70- 3.62 (m, 2H), 3.62-3.54 (m, 1H), 3.54-3.42 (m, 2H), 3.17- 2.97 (m, 3H), 2.97 (s, 3H), 2.86-2.54 (m, 3H), 2.22-2.12 (m, 2H), 2.05-1.97 (m, 2H), 1.72-1.63 (m, 2H), 1.61-1.39 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 451.63 [M + H]⁺. 4

UNC4339A ¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.28 (s, 1H), 7.90 (s, 2H), 4.19-4.10 (m, 1H), 3.70-3.61 (m, 1H), 3.55- 3.42 (m, 4H), 3.00 (t, J = 12.0 Hz, 2H), 3.74 (d, J = 8.0 Hz, 2H), 2.20-2.12 (m, 2H), 2.05- 1.92 (m, 5H), 1.71-1.41 (m, 10H), 1..33 (d, J = 8.0 Hz, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 481.70 [M + H]⁺. 5

UNC4354A ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 4.0 Hz, 1H), 8.37 (s, 1H), 8.04 (dd, J₁ = 4.0 Hz, J₂ = 8.0 Hz, 1H), 7.92 (d, J = 8.0 Hz, 1H), 6.38-6.35 (m, 1H), 4.22-4.12 (m, 1H), 3.89-3.92 (m, 2H), 3.75-3.70 (m, 1H), 3.70-3.63 (m, 2H), 3.59-3.43 (m, 4H), 2.90-2.83 (m, 2H), 2.22-2.12 (m, 2H), 2.08-1.98 (m, 2H), 1.72-1.63 (m, 2H), 1.61-1.39 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 423.58 [M + H]⁺. 6

UNC4356A ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 2.0 Hz, 1H), 8.37 (s, 1H), 8.05 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.92 (d, J = 8.0 Hz, 1H), 6.36-6.32 (m, 1H), 4.20-4.06 (m, 2H), 3.93-3.83 (m, 1H), 3.80-3.72 (m, 1H), 3.72-3.64 (m, 1H), 3.55-3.43 (m, 2H), 3.43-3.35 (m, 1H), 3.02 (s, 3H), 3.01-2.85 (m, 2H), 2.22-2.12 (m, 2H), 2.08- 1.98 (m, 2H), 1.72-1.63 (m, 2H), 1.61-1.39 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 437.60 [M + H]⁺. 7

UNC4358A ¹H NMR (400 MHz, CD₃OD) δ 8.77 (d, J = 2.0 Hz, 1H), 8.38 (s, 1H), 8.08 (dd, J₁ = 2.0 Hz, J₂ = 8.0 Hz, 1H), 7.94 (d, J = 8.0 Hz, 1H), 6.41-6.37 (m, 1H), 4.23-4.10 (m, 1H), 3.99 (s, 1H), 3.82-3.75 (m, 1H), 3.74- 3.62 (m, 2H), 3.56-3.43 (m, 2H), 3.10-2.89 (m, 2H), 2.25- 2.12 (m, 2H), 2.10-1.98 (m, 2H), 1.76-1.38 (m, 14H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 465.66 [M + H]⁺. 8

UNC4387A 1H NMR (400 MHz, CD3OD) δ 8.59 (d, J = 4.0 Hz, 1H), 8.30 (s, 1H), 7.97 (s, 1H), 7.62 (d, J = 8.0 Hz, 1H), 6.72-6.66 (m, 1H), 4.18-4.10 (m, 1H), 3.69- 3.58 (m, 1H), 3.55-3.45 (m, 2H), 3.20-3.15 (m, 2H), 2.94 (s, 6H), 2.30-2.19 (m, 1H), 2.18-2.05 (m, 4H), 2.05-1.97 (m, 2H), 1.71-1.64 (m, 2H), 1.61-1.35 (m, 7H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 479.69 [M + H]⁺. 9

UNC4337A ¹HNMR (400 MHz, CD₃OD) δ 8.51 (s, 1H), 8.29 (s, 1H), 7.88 (s, 2H), 4.19-4.07 (m, 1H), 3.70-3.62 (m, 1H), 3.55-3.40 (m, 4H), 3.02-2.93 (m, 2H), 2.84 (s, 3H), 2.72 (d, J = 8.0 Hz, 2H), 2.20-2.12 (m, 2H), 2.05-1.96 (m, 2H), 1.96-1.89 (m, 3H), 1.71-1.62 (m, 2H), 1.62-1.38 (m, 8H), 1.00 (t, J = 8.0 Hz, 3H). LC-MS (ESI+): t_(R) = 4.484 min, MS m/z 453.0 [M + 1]⁺. 10

UNC4409A 1H NMR (400 MHz, CD3OD) δ 8.59 (d, J = 4.0 Hz, 1H), 8.28 (s, 1H), 7.94 (d, J = 8.0 Hz, 1H), 7.90 (d, J = 8.0 Hz, 1H), 4.18-4.08 (m, 1H), 3.69-3.60 (m, 1H), 3.56-3.42 (m, 4H), 3.21-3.12 (m, 2H), 3.12-3.02 (m, 1H), 2.18-2.09 (m, 4H), 2.05-1.92 (m, 4H), 1.70-1.62 (m, 2H), 1.57-1.38 (m, 6H), 0.99 (t, J = 8.0 Hz, 3H). MS m/z 425.59 [M + H]+. 11

UNC4410A 1H NMR (400 MHz, CD3OD) δ 8.56 (d, J = 4.0 Hz, 1H), 8.36 (s, 1H), 7.94 (s, 1H), 7.51 (d, J = 4.0 Hz, 1H), 4.18-4.09 (m, 1H), 3.67-3.58 (m, 1H), 3.54- 3.45 (m, 2H), 3.06 (d, J = 4.0 Hz, 1H), 2.93 (s, 3H), 2.90 (s, 3H), 2.87-2.70 (m, 2H), 2.31- 2.23 (m, 1H), 2.16-2.08 (m, 2H), 2.05-1.95 (m, 4H), 1.90- 1.71 (m, 4H), 1.70-1.63 (m, 3H), 1.55-1.38 (m, 7H), 0.99 (t, J = 8.0 Hz, 3H). MS m/z 481.70 [M + H]+. 12

UNC4411A 1H NMR (400 MHz, CD3OD) δ 8.58 (d, J = 4.0 Hz, 1H), 8.29 (s, 1H), 7.94-7.87 (m, 2H), 4.18-4.09 (m, 1H), 3.70-3.60 (m, 3H), 3.55-3.42 (m, 2H), 3.24-3.14 (m, 2H), 3.09-2.99 (m, 1H), 2.92 (s, 3H), 2.20- 1.96 (m, 8H), 1.70-1.62 (m, 2H), 1.58-1.38 (m, 6H), 0.99 (t, J = 8.0 Hz, 3H). MS m/z 439.62 [M + H]+. 13

UNC4340A ¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.34 (s, 1H), 7.90-7.83 (m, 2H), 6.56 (s, 1H), 4.20-4.05 (m, 1H), 3.70- 3.58 (m, 2H), 3.58-3.45 (m, 3H), 3.19-3.00 (m, 3H), 2.90- 2.60 (m, 3H), 2.19-2.11 (m, 2 H), 2.05-1.96 (m, 2 H), 1.71- 1.63 (m, 2H), 1.60-1.40 (m, 6H), 1.39 (d, J = 8.0 Hz, 3H), 1.00 (t, J = 8.0 Hz, 3H). LC- MS (ESI+): t_(R) = 4.556 min, MS m/z 479.0 [M + l]⁺.

Example 14 General Procedure for Table 14

A solution of 6-(2-butylamino-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)nicotinaldehyde (370 mg, 1.0 mmol) and 3-(triphenyl-l5-phosphanylidene)pyrrolidine-2,5-dione (360 mg, 1.0 mmol) in MeOH (5.0 mL) was refluxed for 12 hours. The solvent was removed under reduced pressure. The residue was quenched with brine (10 mL) and extracted with DCM (15 mL, 3×). The organic layers were separated. The combined organic layer was dried (MgSO₄) and concentrated. The residue was used in the next step without further purification.

A solution of crude (Z)-3-((6-(2-(butylamino)-4-(((1r,4r)-4-hydroxycyclohexyl)amino) pyrimidin-5-yl)pyridin-3-yl-)methylene)pyrrolidine-2,5-dione (451 mg, 1.0 mmol) in acetic acid (9.0 mL) was added Zn (197 mg, 3.0 mmol). The reaction mixture was refluxed for 1.5 hours. The solvent was then removed under reduced pressure. The residue was quenched with a saturated NaHCO₃ solution (10 mL) and extracted with DCM (15 mL, 3×). The combined organic layer was dried (MgSO₄) and concentrated. The residue was used in the next step without further purification.

A solution of crude 3-((6-(2-(butylamino)-4-((4-hydroxycyclohexyl)amino)pyrimidin-5-yl)pyridin-3-yl)methyl)pyrolidine-2,5-dione (453 mg, 1.0 mmol) in THF (10 mL) was added LiAlH₄ (380 mg, 10.0 mmol). The reaction mixture was refluxed for 2 hours, quenched slowly with a 1.0 N NaOH solution (10 mL) at 0° C., and extracted with DCM (15 mL, 3×). The organic layers were separated. The combined organic layer was dried (MgSO₄) and concentrated. A solution of the residue in MeOH (3.0 mL) was added Pd/C (20 mg). The reaction mixture was open to the air and stirred overnight. The resulting mixture was passed through a pad of celite. The filtrate was concentrated. The residue was purified using HPLC to afford the desired product trans-4-((2-(butylamino)-5-(5-(pyrrolidin-3-ylmethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (27 mg, 5%) (UNC4386A). ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J=4.0 Hz, 1H), 8.27 (s, 1H), 8.05 (d, J=4.0 Hz, 1H), 7.92 (d, J=8.0 Hz, 1H), 4.18-4.10 (m, 1H), 3.69-3.60 (m, 1H), 3.55-3.40 (m, 4H), 3.01-2.85 (m, 3H), 2.76-2.66 (m, 1H), 2.20-2.11 (m, 2H), 2.05-1.98 (m, 2H), 1.83-1.73 (m, 1H), 1.72-1.64 (m, 2H), 1.58-1.38 (m, 6H), 1.00 (t, J=8.0 Hz, 3H). MS m/z 425.59 [M+H]⁺.

Table 14 describes compounds could be prepared following procedures described in Example 14, using appropriate reagents.

1

UNC4386A ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J = 4.0 Hz, 1H), 8.27 (s, 1H), 8.05 (d, J = 4.0 Hz, 1H), 7.92 (d, J = 8.0 Hz, 1H), 4.18-4.10 (m, 1H), 3.69-3.60 (m, 1H), 3.55-3.40 (m, 4H), 3.01-2.85 (m, 3H), 2.76-2.66 (m, 1H), 2.20-2.11 (m, 2H), 2.05-1.98 (m, 2H), 1.83-1.73 (m, 1H), 1.72-1.64 (m, 2H), 1.58-1.38 (m, 6H), 1.00 (t, J = 8.0 Hz, 3H). MS m/z 425.59 [M + H]⁺.

Example 15 UNC2427A General Procedure D:

2,4-Dichloro-N-(4-fluorobenzyl)pyrimidine-5-carboxamide

4-Fluorobenzylamine (1.78 g, 14.2 mmol) in dichloromethane (5.0 mL) was added into a solution of 2,4-dichloropyrimidine-5-carbonyl chloride (3.0 g, 14.2 mmol) in dichloromethane (30 mL) at 0° C. Then N,N-diisopropylethylamine (2.75 g, 21.3 mmol) and 4-(dimethylamino)pyridine (17.1 mg, 0.14 mmol) were added into the mixture. The resulting mixture was allowed to warm to room temperature and stirred for 20 min. The solvent was removed and the residue was dissolved in dichloromethane and washed with water (2×). Solvent was removed and the residue was purified on ISCO to provide the title compound (3.96 g, 93%). ¹H NMR (400 MHz, CD₃OD) δ 8.73 (s, 1H), 7.42-7.35 (m, 2H), 7.12-7.02 (m, 2H), 4.53 (s, 2H); MS m/z 301.30 [M+H]⁺.

(S)-5-((2-((3-Aminopropyl)amino)-5-((4-fluorobenzyl)carbamoyl)pyrimidin-4-yl)amino)-2-((tert-butoxycarbonyl)amino)pentanoic acid

L-Ornithine (232 mg, 1.0 mmol), N,N-diisopropylethylamine (194 mg, 1.5 mmol) were added into a solution of 2,4-dichloro-N-(4-fluorobenzyl)pyrimidine-5-carboxamide (300 mg, 1.0 mmol) in a mixture of isopropyl alcohol and DMF (10 mL, 3:2, v/v) at room temperature. The resulting mixture was stirred for overnight. Then ⅓ of the reaction mixture was added to a solution of 1,3-diaminopropane (304 mg, 4.0 mmol) in DMF (1.0 mL) at room temperature. The reaction mixture was heated at 45° C. for 2 h. The solvent was removed and the residue was purified on HPLC to give the title compound as TFA salt (92 mg, 34%). ¹H NMR (400 MHz, CD₃OD) δ 8.22 (s, 1H), 7.38-7.28 (m, 2H), 7.06-6.95 (m, 2H), 4.45 (s, 2H), 4.18-4.09 (m, 1H), 3.69-3.53 (m, 4H), 3.08-2.99 (m, 2H), 2.05-1.97 (m, 2H), 1.91-1.83 (m, 1H), 1.80-1.66 (m, 3H), 1.41 (s, 9H); MS m/z 534.30 [M+H]⁺.

UNC2427A

O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU, 68.3 mg, 0.21 mmol) and triethylamine (43.5 mg, 0.43 mmol) were added to the solution of (S)-5-((2-((3-aminopropyl)amino)-5-((4-fluorobenzyl)carbamoyl)pyrimidin-4-yl)amino)-2-((tert-butoxycarbonyl)amino)pentanoic acid (70 mg, 0.085 mmol) in DMF (50 mL) The resulting mixture was diluted with dichloromethane (60 mL) and stirred at room temperature for overnight. Then the solvent was removed, the residue was dissolved in dichloromethane (5.0 mL) followed by the addition of TFA (1.0 mL). The resulting mixture was stirred at room temperature for 2.0 h. Then the solvent was removed and the residue was purified on HPLC to provide the title compound (UNC2427A) as TFA salt (27.4 mg, 46%); ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.37-7.26 (m, 2H), 7.06-6.97 (m, 2H), 4.44 (s, 2H), 4.02-3.97 (m, 1H), 3.97-3.89 (m, 1H), 3.81-3.71 (m, 1H), 3.68-3.60 (m, 1H), 3.28-3.12 (m, 2H), 2.87-2.80 (m, 1H), 2.01-1.92 (m, 2H), 1.91-1.82 (m, 1H), 1.80-1.64 (m, 3H). MS m/z 416.25 [M+H]⁺.

Table 15 describes compounds prepared following procedures described in Example 15 (General Procedure D), using appropriate reagents. (Note: MerTK IC50. ++++ means <10 nM; +++ means between 10-100 nM, ++ means between 100 nM-1 μM; + means between 1-30 μM; − means inactive.)

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

UNC2429A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.37-7.29 (m, 2H), 7.07-6.97 (m, 2H), 4.44 (s, 2H), 3.91-3.79 (m, 2H), 3.77-3.69 (m, 1H), 3.65-3.58 (m, 1H), 3.27-3.13 (m, 3H), 2.98-2.92 (m, 4H), 1.94-1.77 (m, 3H), 1.73-1.52 (m, 5H), 1.48-1.34 (m, 3H); MS m/z 444.30 [M + H]⁺. 2

UNC2430A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.20 (d, J = 0.9 Hz, 1H), 7.38-7.29 (m, 2H), 7.07-6.99 (m, 2H), 4.44 (s, 2H), 3.88- 3.66 (m, 4H), 3.51-3.32 (m, 2H), 3.21-3.11 (m, 1H), 2.98- 2.93 (m, 4H), 2.89-2.77 (m, 1H), 1.98-1.85 (m, 2H), 1.84- 1.58 (m, 5H), 1.56-1.48 (m, 1H), 1.46-1.29 (m, 5H); MS m/z 458.30 [M + H]⁺. 3

UNC2479A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 7.36-7.30 (m, 2H), 7.07-6.99 (m, 2H), 4.45 (s, 2H), 3.94-3.85 (m, 1H), 3.80-3.74 (m, 1H), 3.74-3.65 (m, 1H), 3.55-3.45 (m, 2H), 3.38-3.30 (m, 1H), 3.23-3.11 (m, 1H), 2.96 (s, 1H), 2.89- 2.80 (m, 1H), 1.97-1.81 (m, 2H), 1.77-1.55 (m, 5H), 1.54- 1.43 (m, 2H), 1.43-1.21 (m, 7H); MS m/z 472.30 [M + H]⁺. 4

UNC2431A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.22 (s, 1H), 7.37-7.28 (m, 2H), 7.07-6.97 (m, 2H), 4.45 (s, 2H), 3.89-3.79 (m, 2H), 3.71-3.58 (m, 2H), 3.58-3.49 (m, 1H), 3.44-3.34 (m, 1H), 2.95 (s, 1H), 2.90-2.80 (m, 1H), 1.98-1.84 (m, 2H), 1.74- 1.66 (m, 2H), 1.65-1.57 (m, 2H), 1.56-1.51 (m, 1H), 1.50- 1.42 (m, 1H), 1.39-1.25 (m, 8H); MS m/z 486.30 [M + H]⁺. 5

UNC2342A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.44 (d, J = 2.5 Hz, 1H), 7.81-7.73 (m, 2H), 7.53-7.46 (m, 2H), 4.33 (s, 2H), 4.07- 3.93 (m, 4H), 3.82-3.64 (m, 4H), 3.41-3.34 (m, 2H), 3.28- 3.07 (m, 4H), 2.90-2.82 (m, 1H), 2.04-1.95 (m, 2H), 1.94- 1.85 (m, 1H), 1.83-1.68 (m, 3H); MS m/z 483.30 [M + H]⁺. 6

UNC2341A ++ ¹H NMR (400 MHz, CD₃OD) 3 8.45 (s, 1H), 7.81-7.75 (m, 2H), 7.53-7.48 (m, 2H), 4.34 (s, 2H), 4.08-3.98 (m, 2H), 3.92-3.85 (m, 1H), 3.80-3.66 (m, 3H), 3.61-3.52 (m, 1H), 3.47-3.32 (m, 4H), 3.27-3.11 (m, 3H), 2.99-2.96 (m, 1H), 2.95-2.88 (m, 1H), 1.96-1.86 (m, 3H), 1.86-1.75 (m, 2H), 1.72-1.61 (m, 2H), 1.48-1.33 (m, 1H); MS m/z 497.30 [M + H]⁺. 7

UNC2481A + ¹H NMR (400 MHz, CD₃OD) δ 8.17 (s, 1H), 7.37-7.30 (m, 2H), 7.06-7.00 (m, 2H), 4.44 (s, 2H), 3.89-3.78 (m, 2H), 3.77-3.72 (m, 2H), 3.69-3.62 (m, 1H), 3.49-3.33 (m, 3H), 3.02-2.93 (m, 2H), 1.98-1.76 (m, 5H), 1.73-1.62 (m, 3H), 1.60-1.49 (m, 2H); MS m/z 430.30 [M + H]⁺. 8

UNC2483A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.17 (s, 1H), 7.37-7.30 (m, 2H), 7.08-6.99 (m, 2H), 4.45 (s, 2H), 3.91-3.80 (m, 2H), 3.79-3.71 (m, 1H), 3.59-3.51 (m, 1H), 3.48-3.39 (m, 2H), 3.22-3.13 (m, 1H), 2.89-2.80 (m, 1H), 1.94-1.76 (m, 3H), 1.75-1.27 (m, 10H); MS m/z 445.30 [M + H]⁺. 9

UNC2484A +++ 1H NMR (400 MHz, CD₃OD) δ 8.17 (s, 1H), 7.36-7.30 (m, 2H), 7.08-6.99 (m, 2H), 4.45 (s, 2H), 3.81-3.74 (m, 1H), 3.73-3.66 (m, 1H), 3.65-3.59 (m, 2H), 3.53-3.45 (m, 2H), 2.99-2.94 (m, 1H), 2.87-2.82 (m, 1H), 1.90-1.81 (m, 2H), 1.75-1.54 (m, 6H), 1.50-1.31 (m, 5H); MS m/z 458.25 [M + H]⁺. 10

UNC2541A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.18 (s, 1H), 7.36-7.29 (m, 2H), 7.07-6.98 (m, 2H), 4.44 (s, 2H), 3.84 (t, J = 5.6 Hz, 1H), 3.73-3.63 (m, 2H), 3.52- 3.40 (m, 2H), 3.01-2.89 (m, 2H), 1.97-1.84 (m, 2H), 1.75- 1.42 (m, 9H), 1.41-1.29 (m, 5H); MS m/z 472.30 [M + H]⁺. 11

UNC2486A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.37-7.30 (m, 2H), 7.07-6.99 (m, 2H), 4.45 (s, 2H), 3.82-3.75 (m, 1H), 3.75- 3.63 (m, 2H), 3.61-3.54 (m, 1H), 3.48-3.41 (m, 1H), 3.37-3.30 (m, 1H), 2.89-2.80 (m, 1H), 1.93-1.82 (m, 2H), 1.76- 1.60 (m, 4H), 1.57-1.27 (m, 11H); MS m/z 486.30 [M + H]⁺. 12

UNC2487A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.06 (s, 1H), 7.26-7.21 (m, 2H), 6.98-6.90 (m, 2H), 5.28 (s, 2H), 4.39 (s, 2H), 3.39- 3.34 (m, 2H), 3.31-3.23 (m, 3H), 3.20-3.11 (m, 1H), 1.68- 1.56 (m, 4H), 1.56-1.50 (m, 2H), 1.48-1.38 (m, 2H), 1.34- 1.19 (m, 10H); MS m/z 500.35 [M + H]⁺. 13

UNC2573A + ¹H NMR (400 MHz, CD₃OD) δ 8.22 (s, 1H), 7.37-7.29 (m, 2H), 7.06-6.98 (m, 2H), 4.45 (s, 2H), 3.95-3.89 (m, 1H), 3.85-3.75 (m, 1H), 3.70-3.59 (m, 2H), 3.53-3.40 (m, 2H), 2.87-2.77 (m, 1H), 2.36-2.23 (m, 1H), 2.18-2.08 (m, 1H), 2.06-1.95 (m, 1H), 1.72-1.59 (m, 1H); MS m/z 402.20 [M + H]⁺. 14

UNC2574A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 7.38-7.27 (m, 2H), 7.07-6.97 (m, 2H), 4.45 (s, 2H), 4.01-3.95 (m, 1H), 3.94-3.85 (m, 1H), 3.78-3.69 (m, 1H), 3.67-3.57 (m, 1H), 3.46-3.37 (m, 1H), 3.24-3.15 (m, 1H), 3.05-2.91 (m, 5H), 2.20-2.10 (m, 2H), 2.03-1.91 (m, 1H), 1.79-1.69 (m, 2H), 1.63-1.47 (m, 2H); MS m/z 416.25 [M + H]⁺. 15

UNC2575A ++ ¹H NMR (400 MHz, CD₃OD) 5 8.23 (s, 1H), 7.37-7.29 (m, 2H), 7.07-6.98 (m, 2H), 4.45 (s, 2H), 3.92-3.74 (m, 3H), 3.63-3.52 (m, 2H), 3.26-3.21 (m, 1H), 2.96 (s, 1H), 2.89- 2.82 (m, 1H), 2.21-2.13 (m, 2H), 1.74-1.59 (m, 3H), 1.58- 1.43 (m, 3H); MS m/z 430.25 [M + H]⁺. 16

UNC2576A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 7.38-7.29 (m, 2H), 7.07-6.98 (m, 2H), 4.45 (s, 2H), 3.92-3.73 (m, 2H), 3.69-3.59 (m, 2H), 3.52 (ddd, J = 20.6, 13.5, 6.4 Hz, 2H), 3.24-3.10 (m, 2H), 2.98-2.93 (m, 4H), 2.25-2.14 (m, 2H), 1.68-1.59 (m, 3H), 1.55-1.48 (m, 2H), 1.45-1.34 (m, 4H); MS m/z 444.30 [M + H]⁺. 17

UNC2577A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 7.40-7.28 (m, 2H), 7.08-6.97 (m, 2H), 4.45 (s, 2H), 3.88-3.80 (m, 1H), 3.78-3.69 (m, 1H), 3.68-3.53 (m, 3H), 2.93-2.83 (m, 1H), 2.39-2.28 (m, 1H), 2.16-2.04 (m, 1H), 1.71-1.26 (m, 11H); MS m/z 458.30 [M+H]+. 18

UNC2578A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.25 (s, 1H), 7.38-7.29 (m, 2H), 7.07-6.99 (m, 2H), 4.46 (s, 2H), 3.87-3.66 (m, 4H), 3.51-3.43 (m, 1H), 2.91-2.84 (m, 1H), 2.45-2.33 (m, 1H), 2.11-2.03 (m, 1H), 1.67-1.53 (m, 3H), 1.51-1.13 (m, 10H); MS m/z 472.30 [M + H]⁺. 19

UNC2741A ++ ¹H NMR (400 MHz, cd₃od) δ 8.15 (s, 1H), 7.88 (t, J = 5.8 Hz, 1H), 7.38-7.31 (m, 2H), 7.09-7.01 (m, 2H), 4.46 (s, 2H), 3.64-3.55 (m, 2H), 3.44- 3.36 (m, 2H), 3.28-3.23 (m, 2H), 2.20 (t, J = 6.7 Hz, 2H), 1.76-1.60 (m, 7H), 1.59-1.48 (m, 2H), 1.44-1.31 (m, 6H); MS m/z 457.30 [M + H]⁺. 20

UNC2611A ++++ ¹H NMR (400 MHz, cd₃od) δ 8.20 (s, 1H), 7.40-7.29 (m, 2H), 7.08-7.00 (m, 2H), 4.48- 4.44 (m, 2H), 4.44-4.38 (m, 1H), 4.19-4.11 (m, 2H), 3.78- 3.68 (m, 1H), 3.57-3.49 (m, 111), 3.45-3.32 (m. 2H), 2.08- 1.93 (m, 2H), 1.84-1.60 (m, 7H), 1.51-1.26 (m, 5H); MS m/z 473.30 [M + H]⁺. 21

UNC4352A ¹H NMR (400 MHz, CD₃OD) δ 8.17 (s, 1H), 8.02-7.98 (m, 1H), 7.36 (dd, JA = 8.0 Hz, JB = 4.0 Hz, 2H), 7.05 (t, J = 8.0 Hz, 2H), 4.47 (s, 2H), 3.64 (t, J = 6.0 Hz, 2H), 3.40 (t, J = 6.8 Hz, 2H), 2.16 (t, J = 6.4 Hz, 2H), 1.68-1.54 (m, 9H), 1.38- 1.26 (m, 7H); MS m/z 457.30 [M + H]⁺. 22

UNC4378A ¹H NMR (400 MHz, CD₃OD) δ 8.20 (s, 1H), 7.37-7.34 (m, 2H), 7.07-7.03 (m, 2H), 4.46 (s, 2H), 3.79-3.67 (m, 3H), 3.60-3.39 (m, 3H), 2.9-2.95 (m, 2H), 2.66 (s, 3H), 2.02- 1.86 (m, 2H), 1.74-1.58 (m, 6H), 1.54-1.28 (m, 6H); MS m/z 486.30 [M + H]⁺.

Example 16 UNC2324A General Procedure E:

UNC2343A

To a solution of 2,4-dichloropyrimidine-5-carbonyl chloride (500 mg, 2.38 mmol) in dichloromethane (30 mL) was added methanol (87.6 mg, 2.73 mmol) and diisopropylethylamine (369 mg, 2.86 mmol) at 0° C. The resulting mixture was stirred for at 0° C. 1 h. Then the solvent was removed. The residue (412 mg, 2.0 mmol) was dissolved in IPA (20 mL) followed by the addition of L-Ornithine (465 mg, 2.0 mmol) and N,N-diisopropylethylamine (388 mg, 3.0 mmol). The resulting mixture was stirred at 0° C. for 90 min, then dichloromethane (5.0 mL) was added. The resulting mixture was stirred at 0° C. for 1.0 h and at room temperature overnight. Solvent was removed and the residue (MS m/z 403.30 [M+H]⁺) was dissolved in DMF (5.0 mL) and was added dropwise into a solution of 1,4-diaminobutane (1.68 g, 19.1 mmol) in DMF (1.0 mL) at room temperature. The resulting mixture was heated to 45° C. for 1 h. The solvent was removed and the residue was dissolved in ethyl acetate (35 mL) and washed with water (3×). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was purified on HPLC to provide (S)-5-((2-((4-aminobutyl)amino)-5-(methoxycarbonyl)pyrimidin-4-yl)amino)-2-((tert-butoxycarbonyl)amino)pentanoic acid as a semisolid (MS m/z 455.30 [M+H]⁺). The semisolid (595 mg, 1.31 mmol) was dissolved in DMF (150 mL), then TBTU (546.4 mg, 1.70 mmol) and DIEA (508 mg, 3.93 mmol) were added sequentially. The resulting mixture was stirred at room temperature overnight. The solvent was removed. The residue was dissolved in ethyl acetate and washed with water (3×). The organic layer was dried (Na₂SO₄), filtered and concentrated. The residue was purified on HPLC to provide the title compound (UNC2343A). ¹H NMR (400 MHz, CD₃OD) δ 8.42 (s, 1H), 4.08-3.99 (m, 1H), 3.90-3.84 (m, 3H), 3.59-3.47 (m, 2H), 3.46-3.31 (m, 2H), 3.28-3.21 (m, 1H), 3.09-2.95 (m, 1H), 1.90-1.52 (m, 8H), 1.51-1.32 (m, 9H); MS m/z 437.30 [M+H]⁺.

UNC2340A

Lithium hydroxide (200 mg, 8.3 mmol) was added to a solution of UNC2343A (724 mg, 1.66 mmol) in a mixture of THF and H₂O (20 mL, 3:2, v/v). The resulting mixture was heated at 75° C. overnight. Then the reaction mixture was acidified to pH 4, then extracted with a mixture of CH₂Cl₂ and IPA (3:1, v/v) to give the title compound (UNC2340A) (406 mg, 58%). ¹H NMR (400 MHz, CD₃OD) δ 8.36 (s, 1H), 8.11 (s, 1H), 4.12-4.02 (m, 1H), 3.61-3.47 (m, 2H), 3.34 (s, 1H), 3.28-3.17 (m, 1H), 3.06-2.93 (m, 1H), 2.90-2.84 (m, 1H), 1.89-1.52 (m, 7H), 1.42 (s, 9H); MS m/z 423.25 [M+H]⁺.

UNC2324A

4-Fluorobenzylamine (65.1 mg, 0.5 mmol), TBTU (128.2 mg, 0.4 mmol) and triethylamine (68 mg, 0.67 mmol) were added to a solution of UNC2340A (40 mg, 0.095 mmol) in anhydrous DMF (20 mL) at room temperature. The resulting mixture was stirred for 2 h, then solvent was removed, the residue was dissolved in CH₂Cl₂ (30 mL) and washed with water (2×). TFA (1.0 mL) was then added and stirred at room temperature for 2.0 h, condensed and purified on HPLC to provide the title compound (UNC2324A) (26 mg, 52%). ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.37-7.26 (m, 2H), 7.07-6.96 (m, 2H), 4.44 (s, 2H), 3.88-3.82 (m, 1H), 3.77-3.68 (m, 1H), 3.58-3.47 (m, 2H), 3.43-3.35 (m, 1H), 3.26-3.13 (m, 2H), 2.98-2.93 (m, 2H), 2.92-2.84 (m, 1H), 1.92-1.81 (m, 3H), 1.81-1.53 (m, 5H), 1.44-1.29 (m, 1H); MS m/z 430.20 [M+H]⁺.

Table 16 describes compounds prepared following procedures described in Example 16 (General Procedure E), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

UNC2589A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 7.39-7.35 (m, 4H), 4.50-4.47 (m, 2H), 3.97- 3.91 (m, 3H), 3.87-3.83 (m, 1H), 3.40-3.33 (m, 5H), 3.09- 3.01 (m, 4H), 2.87 (s, 4H), 1.93-1.82 (m, 4H), 1.79-1.70 (m, 2H), 1.69-1.57 (m, 3H), 1.44-1.30 (m, 2H); MS m/z 524.40 [M + H]⁺. 2

UNC2615A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.92 (s, 1H), 8.79 (d, J = 5.5 Hz, 1H), 8.67 (d, J = 8.0 Hz, 1H), 8.43 (s, 1H), 8.08 (dd, J = 7.8, 5.9 Hz, 1H), 4.71 (s, 2H), 3.92 (t, J = 5.3 Hz, 1H), 3.76- 3.60 (m, 2H), 3.58-3.36 (m, 2H), 3.38-3.22 (m, 1H), 3.03- 2.89 (m, 1H), 2.05-1.84 (m, 2H), 1.82-1.52 (m, 6H), 1.52- 1.28 (m, 6H); MS (ESI): 455.4 [M + H]⁺. 3

UNC2616A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.81 (d, J = 6.0 Hz, 2H), 8.49 (s, 1H), 8.10 (d, J = 6.1 Hz, 2H), 4.80 (s, 2H), 3.92 (t, J = 5.3 Hz, 1H), 3.82-3.60 (m, 2H), 3.59-3.38 (m, 2H), 3.37- 3.31 (m, 1H), 3.05-2.91 (m, 1H), 2.04-1.83 (m, 2H), 1.82- 1.54 (m, 6H), 1.54-1.23 (m, 6H); MS (ESI): 455.3 [M + H]⁺. 4

UNC2625A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.36 (s, 1H), 4.20-4.03 (m, 1H), 3.91 (t, J = 5.3 Hz, 1H), 3.82-3.61 (m, 2H), 3.60-3.39 (m, 4H), 3.37-3.21 (m, 1H), 3.20-3.04 (m, 2H), 3.04-2.88 (m, 1H), 2.24-2.07 (m, 2H), 2.04-1.81 (m, 4H), 1.81-1.23 (m, 12H); MS (ESI): 447.4 [M + H]⁺. 5

UNC2702A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.78 (d, J = 5.4 Hz, 1H), 8.59 (t, J = 7.6 Hz, 1H), 8.50 (s, 1H), 8.11 (d, J = 8.0 Hz, 1H), 7.99 (t, J = 8.0 Hz, 1H), 4.86 (s, 2H), 3.90 (t, J = 5.3 Hz, 1H), 3.77-3.61 (m, 2H), 3.60-3.38 (m, 2H), 3.35-3.25 (m, 1H), 2.95 (dt, J = 13.2, 4.5 Hz, 1H), 2.02-1.83 (m, 2H), 1.82-1.28 (m, 12H); MS (ESI): 455.4 [M + H]⁺. 6

UNC2626A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.16 (s, 1H), 7.16 (d,J = 8.3 Hz, 1H), 6.53 (d, J = 2.3 Hz, 1H), 6.46 (dd, J = 8.3, 2.4 Hz, 1H), 4.40 (s, 2H), 3.90 (t, J = 5.5 Hz, 1H), 3.83 (s, 3H), 3.77 (s, 3H), 3.73-3.63 (m, 2H), 3.55-3.39 (m, 2H), 2.97 (s, 1H), 2.03-1.83 (m, 2H), 1.77- 1.31 (m, 13H); MS (ESI): 514.3 [M + H]⁺. 7

UNC2701A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.31 (s, 1H), 7.60 (dd, J = 23.0, 8.5 Hz, 4H), 4.54 (s, 2H), 3.90 (t, J = 5.4 Hz, 1H), 3.78- 3.61 (m, 2H), 3.61-3.37 (m, 2H), 3.35-3.31 (m, 1H), 3.27 (s, 6H), 2.99-2.87 (m, 1H), 2.03-1.85 (m, 2H), 1.81-1.55 (m, 6H), 1.55-1.25 (m, 6H); MS (ESI): 497.4 [M + H]⁺. 8

UNC2703A ++++ ¹H NMR (400 MHz, D₂O) δ 8.28 (s, 1H), 7.59 (dd, J = 21.0, 8.7 Hz, 4H), 4.41 (s, 2H), 4.23-4.08 (m, 2H), 4.03 (t, J = 5.7 Hz, 1H), 3.87-3.44 (m, 8H), 3.38-3.23 (m, 3H), 3.09- 3.01 (m, 1H), 2.03-1.90 (m, 2H), 1.83-1.55 (m, 6H), 1.53- 1.27 (m, 6H); MS (ESI): 539.4 [M + H]⁺. 9

UNC2709A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.57 (d, J = 2.5 Hz, 1H), 8.43 (d, J = 1.4 Hz, 1H), 8.23 (s, 1H), 7.99-7.85 (m, 2H), 7.75 (d, J = 1.2 Hz, 1H), 6.53 (dd, J = 2.5, 1.8 Hz, 1H), 4.54 (s, 2H), 3.86 (t, J = 5.5 Hz, 1H), 3.78-3.63 (m, 2H), 3.60- 3.39 (m, 2H), 3.30-3.24 (m, 1H), 2.98-2.89 (m, 1H), 1.99- 1.82 (m, 2H), 1.82-1.20 (m, 12H); MS (ESI): 521.4 [M + H]⁺. 10

UNC2704A ++++ ¹H NMR (400 MHz, D₂O) δ 8.06 (s, 1H), 4.13-3.95 (m, 4H), 3.89-3.74 (m, 2H), 3.72- 3.56 (m, 4H), 3.55-3.39 (m, 2H), 3.36-3.23 (m, 1H), 3.05 (dt, J = 13.4, 4.7 Hz, 1H), 1.96 (dd, J = 13.5, 11.0 Hz, 4H), 1.72-1.60 (m, 6H), 1.53-1.24 (m, 6H); MS (ESI): 448.3 [M + H]⁺. 11

UNC2705A ++++ ¹H NMR (400 MHz, D₂O) δ 8.03 (s, 1H), 4.15-3.93 (m, 3H), 3.91-3.82 (m, 1H), 3.81- 3.41 (m, 8H), 3.39-3.16 (m, 3H), 3.05 (dt, J = 13.5, 4.8 Hz, 1H), 2.03-1.80 (m, 3H), 1.79- 1.49 (m, 7H), 1.49-1.30 (m, 6H); MS (ESI): 462.4 [M + H]⁺. 12

UNC2706B ++++ ¹H NMR (400 MHz, D₂O) δ 8.23 (s, 1H), 7.46 (d, J = 8.8 Hz, 2H), 7.17 (d, J = 8.7 Hz, 2H), 4.03 (t, J = 5.4 Hz, 1H), 3.88 (d, J = 12.5 Hz, 2H), 3.78-3.43 (m, 6H), 3.25 (dd, J = 42.0, 11.7 Hz, 5H), 3.12- 2.93 (m, 4H), 2.06-1.85 (m, 2H), 1.85-1.56 (m, 6H), 1.56- 1.23 (m, 6H); MS (ESI): 538.4 [M + H]⁺. 13

UNC2834A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.42-8.23 (m, 1H), 7.60 (s, 2H), 7.50 (s, 3H), 4.49-4.30 (m, 2H), 4.19-4.02 (m, 1H), 3.93 (s, 1H), 3.78-3.62 (m, 2H), 3.65-3.40 (m, 4H), 3.31- 3.10 (m, 3H), 2.96 (d, J = 13.3 Hz, 1H), 2.26-1.83 (m, 6H), 1.82-1.56 (m, 6H), 1.57-1.26 (m, 6H); MS (ESI): 537.4 [M + H]⁺. 14

UNC2835A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.00 (s, 1H), 3.95-3.87 (m, 1H), 3.86-3.76 (m, 2H), 3.76- 3.61 (m, 2H), 3.59-3.39 (m, 2H), 3.31-3.24 (m, 3H), 3.15 (s, 3H), 3.01-2.90 (m, 1H), 2.75 (s, 3H), 2.04-1.85 (m, 2H), 1.86-1.55 (m, 6H), 1.53- 1.28 (m, 6H); MS (ESI): 435.4 [M + H]⁺. 15

UNC2836A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.31 (s, 1H), 7.62 (dd, J = 35.5, 8.1 Hz, 4H), 4.54 (s, 2H), 4.19-4.01 (m, 4H), 3.91 (s, 1H), 3.79-3.60 (m, 6H), 3.59- 3.41 (m, 2H), 3.30-3.25 (m, 1H), 3.02-2.87 (m, 1H), 2.04- 1.84 (m, 2H), 1.84-1.55 (m, 6H), 1.51-1.28 (m, 6H); MS (ESI): 539.4 [M + H]⁺. 16

UNC2837A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.41 (s, 1H), 8.24 (s, 1H), 7.89 (s, 2H), 7.72 (s, 1H), 6.50 (s, 1H), 4.52 (s, 2H), 4.08 (t, J = 4.7 Hz, 1H), 3.73-3.53 (m, 3H), 3.48-3.32 (m, 2H), 3.09-2.98 (m, 1H), 1.87-1.20 (m, 14H); MS (ESI): 544.3 [M + Na]⁺. 17

UNC2910A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.35 (s, 1H), 7.65-7.55 (m, 2H), 7.52-7.43 (m, 3H), 6.33- 6.12 (m, 2H), 5.86-5.68 (m, 2H), 4.34 (s, 2H), 4.26-3.88 (m, 5H), 3.76-3.42 (m, 5H), 3.16 (t, J = 12.4 Hz, 2H), 2.24-2.14 (m, 2H), 2.05-1.89 (m, 3H), 1.66-1.33 (m, 4H), 1.24-1.13 (m, 1H); MS (ESI): 533.4 [M + H]⁺. 18

UNC2967A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.48-8.37 (m, 1H), 8.21 (s, 1H), 7.54-7.40 (m, 4H), 4.43- 4.21 (m, 2H), 4.05 (t, J = 11.7 Hz, 1H), 3.96 (s, 1H), 3.89- 3.62 (m, 4H), 3.53 (d, J = 12.7 Hz, 2H), 3.43-3.34 (m, 2H), 3.12 (t, J = 12.4 Hz, 2H), 2.89-2.78 (m, 1H), 2.29-1.93 (m, 3H), 1.93-1.44 (m, 8H), 1.44-1.27 (m, 4H); MS (ESI): 523.4 [M + H]⁺. 19

UNC2968A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.27 (s, 1H), 7.37 (dd, J = 8.5, 5.4 Hz, 2H), 7.05 (t, J = 8.7 Hz, 2H), 4.47 (s, 2H), 3.96-3.68 (m, 4H), 3.49-3.34 (m, 2H), 2.92-2.81 (m, 1H), 2.05 1.62 (m, 6H), 1.62-1.29 (m, 6H); MS (ESI): 458.3 [M + H]⁺ 20

UNC3038A ++++ ¹H NMR (400 MHz, CD₃OD) δ 8.33 (s, 1H), 4.11 (s, 1H), 3.90 (t, J = 5.4 Hz, 1H), 3.79- 3.65 (m, 3H), 3.62-3.38 (m, 3H), 3.29-3.23 (m, 1H), 3.22- 2.84 (m, 5H), 2.33-1.83 (m, 6H), 1.78-1.57 (m, 6H), 1.53- 1.30 (m, 6H), 1.20-1.10 (m, 1H), 0.86-0.69 (m, 2H), 0.54- 0.37 (m, 2H); MS (ESI): 501.4 [M + H]⁺. 21

UNC2914A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.62 (d, J = 2.7 Hz, 1H), 8.48 (d, J = 2.0 Hz, 1H), 8.37 (s, 1H), 8.15 (dd, J = 8.6, 2.2 Hz, 1H), 8.03 (d, J = 8.6 Hz, 1H), 7.85 (d, J = 1.5 Hz, 1H), 7.35 (d, J = 8.1 Hz, 2H), 7.27 (d, J = 8.1 Hz, 2H), 6.62 (dd, J = 2.6, 1.8 Hz, 1H), 4.74 (d, J = 13.7 Hz, 1H), 4.60-4.48 (m, 4H), 3.95-3.83 (m, 2H), 3.76- 3.55 (m, 1H), 3.43-3.32 (m, 1H), 3.28-3.15 (m, 1H), 1.86- 1.72 (m, 2H), 1.31-1.10 (m, 2H), 1.03-0.88 (m, 1H), 0.56- 0.43 (m, 1H). MS m/z 541.3 [M + H]⁺. 22

UNC2916A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.35 (s, 1H), 7.62-7.53 (m, 2H), 7.53-7.46 (m, 3H), 7.40- 7.33 (m, 2H), 7.31-7.23 (m, 2H), 4.81-4.71 (m, 1H), 4.61- 4.49 (m, 2H), 4.46 (s, 1H), 4.33 (s, 2H), 4.12-3.99 (m, 1H), 3.94-3.82 (m, 2H), 3.77- 3.67 (m, 1H), 3.62-3.47 (m, 2H), 3.45-3.33 (m, 2H), 3.26- 3.08 (m, 4H), 2.23-2.11 (m, 2H), 2.01-1.87 (m, 2H), 1.77 (dd, J = 13.4, 7.9 Hz, 2H), 1.28-1.10 (m, 3H), 1.03-0.87 (m, 1H), 0.57-0.42 (m, 1H). MS m/z 557.35 [M + H]⁺.

Example 17 UNC3263A General Procedure F:

2,4-Dichloro-N-[(4-fluorophenyl)methyl]pyrimidine-5-carboxamide

A solution of 2,4-dichloropyrimidine-5-carbonyl chloride (3.35 g, 15.8 mmol) in dichloromethane (53 mL) was added (4-fluorophenyl)methanamine (1.32 g, 10.56 mmol) and DIEA (3.7 mL, 21 mmol) at 0° C. The resulting mixture was stirred at 0° C. for 1 h, the solvent was removed, and the residue was purified by ISCO silica gel column to provide the title compound (1.97 g, 62%) as a yellow solid.

N-[(4-Fluorophenyl)methyl]-4-[(4-hydroxyhept-6-en-1-yl)amino]-2-[(oct-7-en-1-yl)amino]pyrimidine-5-carboxamide

A solution of 2,4-dichloro-N-[(4-fluorophenyl)methyl]pyrimidine-5-carboxamide (97 mg, 0.325 mmol) in i-PrOH (5 mL) was added 7-aminohept-1-en-4-ol (42 mg, 0.325 mmol) and DIEA (85 μL, 0.488 mmol) at 0° C. The mixture was allowed to warm to room temperature and stirred overnight. To the reaction was added oct-7-en-1-amine (207 mg, 0.975 mmol) and DIEA (85 μL, 0.488 mmol). The reaction was heated at 70° C. for 6 h and the volatiles were removed under a reduced pressure. The residue was dissolved in CH₂Cl₂ (4.0 mL) and washed with H₂O (2.0 mL). The H₂O layer was extracted with CH₂Cl₂ (2×20 mL); the organic layers were combined, dried (Na₂SO₄), and the solvent was removed under a reduced pressure. The residue was purified by ISCO silica gel column to provide the title compound (39 mg, 25%) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 8.70 (s, 1H), 8.09 (s, 1H), 7.29 (dd, J=8.7, 5.3 Hz, 2H), 7.07-6.98 (m, 2H), 6.08 (s, 1H), 5.90-5.71 (m, 2H), 5.18-5.04 (m, 1H), 5.03-4.89 (m, 2H), 4.51 (d, J=5.7 Hz, 2H), 3.70 (s, 1H), 3.49 (s, 2H), 3.38 (dt, J=9.7, 4.8 Hz, 2H), 2.35-2.12 (m, 2H), 1.80-1.68 (m, 2H), 1.59 (s, 9H), 1.44-1.31 (m, 5H).

N-[(4-Fluorophenyl)methyl]-6-hydroxy-2,16,18,21-tetraazabicyclo[15.3.1]henicosa-1(20),17(21),18-triene-20-carboxamide (UNC3263A)

A solution of N-[(4-fluorophenyl)methyl]-4-[(4-hydroxyhept-6-en-1-yl)amino]-2-[(oct-7-en-1-yl)amino]pyrimidine-5-carboxamide (34 mg, 0.07 mmol) in toluene (35 mL) was added benzoquinone (1.5 mg, 0.014 mmol) and Grubb's 2^(nd) generation catalyst (6.0 mg, 0.007 mmol). The mixture was refluxed under Ar overnight. After which more catalyst was added (6.0 mg), and heated at reflux for 8 h. The volatiles were removed and the residue was purified by ISCO silica gel column to provide the RCM product as a crude brown solid. The residue was dissolved in MeOH (1.0 mL) and Pd/C (10 mg) was added. The mixture was stirred at room temperature under a hydrogen atmosphere for 24 h. The mixture was filtered through Celite and washed with MeOH then purified by HPLC to afford the title compound as a white solid (5.3 mg, 16%). ¹H NMR (400 MHz, CD₃OD) δ 8.21 (s, 1H), 7.37 (dd, J=8.8, 5.4 Hz, 2H), 7.05 (t, J=8.8 Hz, 2H), 4.47 (s, 2H), 3.73-3.60 (m, 2H), 3.58-3.41 (m, 3H), 1.84-1.72 (m, 2H), 1.72-1.62 (m, 2H), 1.61-1.45 (m, 5H), 1.43-1.26 (m, 11H). MS m/z 458.3 [M+H]⁺.

Table 17 describes compounds prepared following procedures described in Example 17 (General Procedure F), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound ID IC₅₀ or/and ¹H NMR 1

UNC3388A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.40-7.32 (m, 2H), 7.09-7.02 (m, 2H), 4.47 (s, 2H), 3.85-3.70 (m, 3H), 3.67-3.55 (m, 1H), 1.90-1.42 (m, 14H). MS m/z 402.3 [M + H]⁺. 2

UNC3429A +++ ¹H NMR (400 MHz, CD₃OD) δ 8.19 (s, 1H), 7.37 (dd, J = 8.7, 5.4 Hz, 2H), 7.06 (t, J = 8.8 Hz, 2H), 4.47 (s, 2H), 3.81-3.70 (m, 1H), 3.66-3.55 (m, 2H), 3.54-3.46 (m, 1H), 3.45-3.35 (m, 1H), 1.85-1.72 (m, 1H), 1.72-1.59 (m, 3H), 1.58-1.30 (m, 14H). MS m/z 444.3 [M + H]⁺. 3

UNC3431A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.20 (s, 1H), 7.37 (dd, J = 8.7, 5.4 Hz, 2H), 7.05 (t, J = 8.8 Hz, 2H), 4.47 (s, 2H), 3.59 (dd, J = 13.8, 6.7 Hz, 3H), 3.53-3.40 (m, 2H), 1.77-1.60 (m, 5H), 1.60-1.27 (m, 18H). MS m/z 472.3 [M + H]⁺. Table 18 describes compounds can be prepared following procedures described in Example 17 (General Procedure F), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

2

3

4

5

Example 18 UNC3017A, UNC3018A & UNC3019A General Procedure G:

(S)-6-((2-(6-Aminohexyl)amino)-5-bromopyrimidin-4-yl)amino)-2-((tert-butoxycarbonyl)amino)hexanoic acid

A solution of (S)-6-amino-2-((tert-butoxycarbonyl)amino)hexanoic acid (0.042 g, 0.10 mmol) in DMSO was added hexane-1,6-diamine (0.046 g, 0.40 mmol). The resulting mixture was heated at 100° C. for 2 h. After cooled to room temperature, the solvent was removed under reduced pressure. The resulting residue was purified by reverse phase ISCO column to provide title compound (0.041 g, 79%). ¹H NMR (400 MHz, CD₃OD) δ 7.91 (s, 1H), 4.13-4.02 (m, 1H), 3.57 (t, J=12, 2H), 3.51-3.38 (bs, 2H), 2.94 (t, J=12, 2H), 1.92-1.80 (m, 1H), 1.75-1.62 (m, 7H), 1.57-1.36 (m, 15H); MS m/z 517.3 [M+H]⁺.

A solution of (S)-6-((2-((6-aminohexyl)amino)-5-bromopyrimidin-4-yl)amino)-2-((tert-butoxycarbonyl)amino)hexanoic acid (2.11 g, 4.08 mmol) and DIEA (1.78 mL, 10.19 mmol) in 20 mL DMF and a solution of HATU (2.01 g, 5.28 mmol) in 20 mL DMF were added to 200 mL of DMF in 16 h. After addition, the resulting mixture was stirred for 1 h. The solvent was removed under reduced pressure. The residue was purified by ISCO silica gel column to provide the desired bromide (0.87 g, 43%) containmated with small amount of impurities. MS m/z 499.3 [M+H]⁺.

A solution of the bromide (0.66 g, 1.32 mmol) in DMF (6.6 mL) was added PdCl₂(dppf).CH₂Cl₂ (0.11 g, 0.13 mmol), CuBr (0.036 g, 0.26 mmol), K₂CO₃ (0.56 g, 9.96 mmol), (5-(1,3-dioxolan-2-yl)pyridin-2-yl)boronic acid lithium hydroxide (0.86 g, 9.96 mmol) and H₂O (1.7 mL) at room temperature. The resulting mixture was heated at 120° C. for 30 min under. After cooled to room temperature, the mixture was filtered over Celite. The solvents were removed under reduced pressure. The crude residue was purified by ISCO silica gel column to provide the desired acetal (0.76 g, 63%) containmated with small amount of impurities. MS m/z 570.4 [M+H]⁺.

A solution of the acetal (0.47 g, 0.83 mmol) in acetone (10 mL) was added p-TsOH.H₂O (0.24 g, 1.25 mmol) and H₂O (2.0 mL). After stirring at room temperature for 16 h, the reaction mixture was quenched with a sat. aq solution of NaHCO₃ and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The resulting residue was purified by ISCO silica gel column to provide the desired aldehyde (0.42 g, 96%) containmated with small amount of impurities. MS m/z 526.4 [M+H]⁺.

UNC3017A

A solution of the aldehyde (0.53 g, 0.1 mmol) in CH₂Cl₂ (2.0 mL) was added morpholine (0.013 mL, 0.15 mmol) and acetic acid (0.04 mL) The resulting solution was stirred at room temperature for 2 h, then NaB(OAc)₃H (0.043 g, 0.15 mmol) was added. After stirred at room temperature for 16 h, the reaction was quenched with a sat. aq. solution of NaHCO₃ and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was dissolved in a mixture of CH₂Cl₂ (2.0 mL) and TFA (1.0 mL) After stirred at room temperature for 2.0 h. the reaction was concentrated and the residue was purified by prep-HPLC to provide the desired product UNC3017A (0.046 g, 93%). ¹H NMR (400 MHz, CD₃OD) δ 8.88 (s, 1H), 8.41 (s, 1H), 8.22 (d, J=8.4 Hz, 1H), 8.01 (d, J=8.4 Hz, 1H), 4.52 (s, 2H), 4.06 (d, J=10.7 Hz, 2H), 3.96-3.79 (m, 4H), 3.77-3.67 (m, 1H), 3.57 (td, J=12.2, 5.2 Hz, 2H), 3.45 (d, J=12.4 Hz, 2H), 3.39-3.23 (m, 3H), 3.02-2.93 (m, 1H), 1.96 (dd, J=10.2, 4.6 Hz, 2H), 1.86-1.51 (m, 7H), 1.42 (d, J=4.7 Hz, 5H); MS m/z 497.4 [M+H]⁺.

UNC3018A

A solution of the above aldehyde (0.53 g, 0.1 mmol) in CH₂Cl₂ (2.0 mL) was added N-methylpiperazine (0.017 mL, 0.15 mmol) and acetic acid (0.04 mL) The resulting solution was stirred at room temperature for 2 h, then NaB(OAc)₃H (0.043 g, 0.15 mmol) was added. After stirred at room temperature for 16 h, the reaction was quenched with a sat. aq. solution of NaHCO₃ and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was dissolved in a mixture of CH₂Cl₂ (2.0 mL) and TFA (1.0 mL) After stirred at room temperature for 2.0 h. the reaction was concentrated and the residue was purified by prep-HPLC to give the desired product UNC3018A (0.049 g, 98%). ¹H NMR (400 MHz, CD₃OD) δ 8.91 (d, J=1.7 Hz, 1H), 8.40 (s, 1H), 8.27 (dd, J=8.5, 2.0 Hz, 1H), 8.01 (d, J=8.5 Hz, 1H), 4.61 (s, 2H), 3.91 (t, J=5.4 Hz, 1H), 3.88-3.61 (m, 10H), 3.61-3.51 (m, 2H), 3.39-3.34 (m, 1H), 3.02 (s, 3H), 3.00-2.92 (m, 1H), 2.03-1.89 (m, 2H), 1.87-1.50 (m, 7H), 1.48-1.35 (m, 5H); MS m/z 510.4 [M+H]⁺.

UNC3019A

A mixture of aldehyde (0.053 g, 0.1 mmol) in 10 mL tBuOH was added NaClO₂ (0.034 g, 80%, 0.3 mmol), NaH₂PO₄ (0.041 g, 0.3 mmol), 2-Me-2-Butene (0.11 mL, 1 mmol) and 2 mL H₂O. After stirring 16 h at room temperature, the reaction was quenched with sat. aq. Na₂S₂O₃, acidified with diluted aq. HCl to pH 4 and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was dissolved in 3 mL DMF. To this solution was added HATU (0.042 g, 0.11 mmol), followed by N,1-dimethylpiperidin-4-amine (0.014 g, 0.11 mmol). After stirring for 16 at room temperature, the reaction mixture was condensed under vacuum and purified by Prep-HPLC. The Boc protected intermediate was dissolved in 2 mL CH₂Cl₂ and 1 mL TFA and stirred for 2 h. After evaporating the solvents, the residue was purified by Prep-HPLC to provide the desired product UNC3019A (0.026 g, 47%). ¹H NMR (400 MHz, CD₃OD) δ 8.70 (s, 1H), 8.41 (s, 1H), 8.02-7.93 (m, 2H), 3.92-3.50 (m, 8H), 3.39-3.33 (m, 1H), 3.23 (bs, 1H), 3.10-2.75 (m, 8H), 2.24 (dd, J=24.3, 11.4 Hz, 2H), 2.15-2.02 (m, 2H), 2.02-1.88 (m, 2H), 1.87-1.48 (m, 8H), 1.45-1.37 (m, 4H); MS m/z 552.4 [M+H]⁺.

Example 19 UNC3588A General Procedure H:

5-Bromo-N2-(but-3-en-1-yl)-N4-(5-((tert-butyldimethylsilyl)oxy)dec-9-en-1-yl)pyrimidine-2,4-diamine

A solution of 5-bromo-2,4-dichloropyrimidine (0.29 g, 1.28 mmol) in isopropanol (3.0 mL) was added 5-((tert-butyldimethylsilyl)oxy)dec-9-en-1-amine (0.38 g, 1.34 mmol) and DIEA (0.27 mL, 1.54 mmol) at 0° C. The reaction solution was stirred at room temperature for 3 h. The solvent was removed under a reduced pressure to provide a yellow residue, which was dissolved in DMSO (5.0 mL). But-3-en-1-amine (0.47 mL, 5.12 mmol) was added. The resulting mixture was heated at 110° C. for 16 h, then diluted with Et₂O and quenched with brine. The aqueous layer was extracted with Et₂O (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was purified by ISCO silica gel column to provide desired product (0.58 g, 89%). ¹H NMR (400 MHz, CDCl₃) δ 7.85 (s, 1H), 5.91-5.72 (m, 2H), 5.18-4.91 (m, 5H), 4.85 (t, J=4.9 Hz, 1H), 3.65 (p, J=5.4 Hz, 1H), 3.47-3.37 (m, 4H), 2.34 (qt, J=6.8, 1.3 Hz, 2H), 2.03 (q, J=6.5 Hz, 2H), 1.64-1.53 (m, 2H), 1.51-1.33 (m, 8H), 0.88 (s, 9H), 0.04 (s, 3H), 0.03 (s, 3H); MS m/z 511.3 [M+H]⁺.

UNC3588A

A solution of 5-bromo-N²-(but-3-en-1-yl)-N⁴-(5-((tert-butyldimethylsilyl)oxy)dec-9-en-1-yl)pyrimidine-2,4-diamine (0.26 g, 0.50 mmol) and benzoquinone (0.009 g, 0.08 mmol) in toluene (20 mL) was added Grela's catalyst (0.027 g, 0.04 mmol) in toluene (5.0 mL) over 1.0 h at 110° C. The resulting dark brown solution was heated at 110° C. for another hour. After cooled to 60° C., 2-mercaptonicotinic acid (0.39 g, 2.5 mmol) was added and stirred at 60° C. for 2 h. After cooled to room temperature, the reaction mixture was filtered over Celite and washed with CH₂Cl₂. The filtrate was concentrated and the residue was purified by ISCO silica gel column to provide the macrocyclic intermediate as a mixture of E and Z olefin isomers (0.19 g, 80%). MS m/z 483.3 [M+H]⁺.

A schlenk flask containing LiCl (0.028 g, 0.66 mmol) and stir bar was flame dried. After cooled to room temperature, CuCl (0.054 g, 0.55 mmol) and Pd(PPh₃)₄ (0.013 g, 0.011 mmol) was added. The reaction mixture was vacuumed and refilled with argon (4×). The intermediate from previous step (0.054 g, 0.11 mmol) in DMSO (4.0 mL), and Bu₃SnPy (0.049 g, 0.13 mmol) were added under argon. The resulting reaction mixture was freeze-thawed under argon (4×). The mixture was heated at 60° C. for 2 d, then diluted with EtOAc, quenched with brine and a saturated aq. solution of NaHCO₃. The organic layer was washed with a sat. aq solution of NaHCO₃ (3×). The combined aqueous layers were extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was purified by ISCO silica gel column to provide Stille coupling products (0.040 g, 75%). MS m/z 482.4 [M+H]⁺.

A solution of the Stille coupling product (0.040 g, 0.083 mmol) in MeOH (5.0 mL) was added a conc. HCl solution (0.50 mL) The resulting mixture was stirred for 1 h and concentrated under reduced pressure. After zoetrope with MeOH (3×), the residue was dissolved in MeOH (5.0 mL) and AcOH (0.50 mL) and was added Pd/C (0.009 g, 10 wt %). The reaction mixture was stirred at room temperature under hydrogen for 1 d, then filtered over Celite and washed with MeOH. The filtrate was concentrated and the residue was purified by reverse-phase HPLC to provide the desired product UNC3588A (0.025 g, 82% over 2 steps). ¹H NMR (400 MHz, CD₃OD) δ 8.62 (ddd, J=5.0, 1.6, 0.9 Hz, 1H), 8.28 (s, 1H), 7.96-7.82 (m, 2H), 7.39 (ddd, J=7.3, 5.0, 1.1 Hz, 1H), 3.91-3.79 (m, 1H), 3.71-3.53 (m, 3H), 3.49-3.38 (m, 1H), 1.92-1.78 (m, 1H), 1.76-1.65 (m, 3H), 1.62-1.34 (m, 14H). MS m/z 370.3 [M+H]⁺.

Table 19 describes compounds can be prepared following procedures described in Example 19 (General Procedure H), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound ID IC₅₀ or/and ¹H NMR 1

UNC3737A ¹H NMR (400 MHz, CD₃OD) δ 8.82 (dd, Ja = 5.2 Hz, Jb = 0.8 Hz, 1H), 8.35 (td, Ja = 8.0 Hz, Jb = 1.6 Hz, 1H), 8.17 (s, 1H), 8.04 (d, J = 8.4 Hz, 1H), 7.81-7.78 (m, 1H), 3.82-3.75 (m, 2H), 3.69-3.64 (m, 1H) 3.36-3.32 (m, 3H), 1.83-1.52 (m, 12H), 1.41-1.33 (m, 2H); MS m/z 328.25 [M + H]⁺ 2

UNC3724A ¹H NMR (400 MHz, CD₃OD) δ 8.63 (d, J = 4.8 Hz, 1H), 8.26 (s, 1H), 7.96-7.91 (td, Ja = 8.4 Hz, Jb = 2.0 Hz, 1H), 7.86 (d, J = 8.4 Hz, 1H), 7.42- 7.38 (m, 1H), 4.00-3.92 (m, 3H), 3.83-3.66 (m, 3H) 3.54- 3.38 (m, 2H), 1.82-1.28 (m, 15H); MS m/z 342.25 [M + H]⁺ 3

UNC3722A ¹H NMR (400 MHz, CD₃OD) δ 8.88 (d, J = 5.6 Hz, 1H), 8.50 (t, J = 8.0 Hz, 1H), 8.12- 8.10 (m, 2H), 7.94 (dd, Ja = 7.2 Hz, Jb = 5.6 Hz, 1H), 3.80-3.77 (m, 1H), 3.65-3.58 (m, 1H), 3.56-3.49 (m, 3H), 1.71-1.36 (m, 15H); MS m/z 356.30 [M + H]⁺ 4

UNC3727A ¹H NMR (400 MHz, CD₃OD) δ 8.84 (d, J = 5.2 Hz, 1H), 8.42 (t, J = 7.6 Hz, 1H), 8.16 (s, 1H), 8.09 (d, J = 8.0 Hz, 1H), 7.85 (t, J = 6.4 Hz, 1H), 3.68-3.64 (m, 3H), 3.55-3.48 (m, 2H), 1.81-1.65 (m, 4H), 1.63-1.39 (m, 14H); MS m/z 370.30 [M + H]⁺ 5

UNC3739A ¹H NMR (400 MHz, CD₃OD) δ 8.84 (s, 1H), 8.41 (br, 1H), 8.15 (s, 1H), 8.07 (br, 1H), 7.86 (br, 1H), 3.84-3.80 (m, 1H), 3.67-3.52 (m, 4H), 1.74- 1.67 (m, 6H), 1.57-1.42 (m, 8H); MS m/z 342.25 [M + H]⁺ 6

UNC3723A ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 5.2 Hz, 1H), 8.24-8.19 (m, 2H), 7.98 (d, J = 8.4 Hz, 1H), 7.69-7.66 (m, 1H), 3.82-3.75 (m, 1H), 3.69- 3.57 (m, 2H), 3.48-3.42 (m, 2H), 1.84-1.40 (m, 16H); MS m/z 356.30 [M + H]⁺ 7

UNC3738A ¹H NMR (400 MHz, CD₃OD) δ 8.76 (d, J = 5.6 Hz, 1H), 8.25-8.20 (m, 2H), 7.99 (d, J = 8.0 Hz, 1H), 7.69-7.66 (dd, Ja = 6.8 Hz, Jb = 5.6 Hz, 1H), 3.69-3.62 (m, 3H), 3.53-3.49 (m, 2H), 1.74-1.69 (m, 5H), 1.50-1.34 (m, 17H); m/z 384.30 [M + H]⁺ 8

9

UNC3726A ¹H NMR (400 MHz, CD₃OD) δ 8.73 (d, J = 5.2 Hz, 1H), 8.21-8.15 (m, 2H), 7.96 (d, J = 8.0 Hz, 1H), 7.63 (dd, Ja = 7.2 Hz, Jb = 5.6 Hz, 1H), 3.78- 3.71 (m, 1H), 3.65-3.58 (m, 3H), 3.50-3.43 (m, 2H), 1.82- 1.70 (m, 5H), 1.53-1.42 (m, 13H); m/z 370.30 [M + H]⁺ 10

UNC3725A ¹H NMR (400 MHz, CD₃OD) δ5 8.80 (d, J = 4.8 Hz, 1H), 8.35 (t, J = 7.2 Hz, 1H), 8.18 (s, 1H), 8.04 (d, J = 8.0 Hz, 1H), 7.81-7.78 (m, 1H), 3.70- 3.65 (m, 2H), 3.57-3.46 (m, 3H), 1.73-1.69 (m, 4H), 1.55- 1.42 (m, 16H); m/z 384.30 [M + H]⁺ 11

UNC3728A ¹H NMR (400 MHz, CD₃OD) δ 8.75 (d, J = 4.4 Hz, 1H), 8.21-8.19 (m, 2H), 7.99 (d, J = 8.0 Hz, 1H), 7.66 (m, 1H), 3.67-3.48 (m, 6H), 1.75-1.67 (m, 4H), 1.49-1.39 (m, 17H); m/z 398.30 [M + H]⁺

Example 20 UNC3295A General Procedure I:

A solution of the bromide intermediate (0.17 g, 0.34 mmol) in DMF (2.0 mL) was added Pd(dppf)Cl₂.CH₂Cl₂ (0.028 g, 0.034 mmol), CuBr (0.098 g, 0.68 mmol), K₂CO₃ (0.14 g, 1.02 mmol), (5-(1,3-dioxolan-2-yl)pyridin-2-yl)boronic acid lithium hydroxide (0.22 g, 1.02 mmol) and water (0.50 mL). The resulting mixture was heated at 120° C. for 30 min open to air. The mixture was filtered over Celite at room temperature. The solvents were removed under a reduced pressure and the residue was purified by ISCO silica gel column to provide the desired coupling product (0.053 g, 28%) contaminated with small amount impurities; MS m/z [M+H]⁺.

A solution of the coupling product (0.053 g, 0.10 mmol) in acetone (10 mL) was added p-TsOH.H₂O (0.029 g, 0.15 mmol) and H₂O (0.80 mL) The reaction mixture was stirred at room temperature for 16 h, then quenched with a sat. aq solution of NaHCO₃ and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The resulting residue was purified by ISCO silica gel column to provide the desired aldehyde intermediate (0.031 g, 78%) contaminated with small amount impurities; MS m/z 554.4 [M+H]⁺.

A solution of the aldehyde (0.031 g, 0.078 mmol) in CH₂Cl₂ (2.0 mL) was added morpholine (0.01 mL, 0.12 mmol) and 0.08 mL acetic acid. The resulting solution was stirred at room temperature for 2 h, then NaB(OAc)₃H (0.033 g, 0.16 mmol) was added. The reaction mixture was stirred at room temperature for 16 h, quenched by a sat. aq. solution of NaHCO₃ and extracted with EtOAc (3×). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was dissolved in MeOH (5.0 mL) and was added Pd/C (0.015 g, 5 wt % Pd/C). The reaction mixture was stirred under hydrogen atmosphere at room temperature for 16 h, then filtrated over Celite and washed with MeOH. The filtrate was concentrated and the residue was purified with reverse-phase HPLC to provide the desired product UNC3295A (0.0096 g, 26%). ¹H NMR (400 MHz, CD₃OD) δ 8.73 (d, J=1.8 Hz, 1H), 8.40 (s, 1H), 8.06 (dd, J=8.5, 2.2 Hz, 1H), 7.96 (d, J=8.5 Hz, 1H), 4.40 (s, 2H), 3.98-3.80 (m, 5H), 3.70-3.51 (m, 3H), 3.49-3.38 (m, 1H), 3.29 (bs, 4H), 1.90-1.79 (m, 1H), 1.77-1.65 (m, 3H), 1.62-1.36 (m, 14H); MS m/z 469.4 [M+H]⁺.

Table 20 describes compounds prepared following procedures described in Example 20 (General Procedure I), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

+++ ¹H NMR (400 MHz, CD₃OD) 8 8.49 (d, J = 1.3 Hz, 1H), 8.28 (s, 1H), 7.80-7.71 (m, 2H), 4.63 (s, 2H), 3.83-3.72 (m, 1H), 3.66-3.56 (m, 1H), 3.56-3.41 (m, 2H), 3.39-3.33 (m, 1H), 1.87-1.74 (m, 1H), 1.71-1.58 (m, 4H), 1.56-1.36 (m, 13H); MS m/z 400.3 [M + H]⁺. 2

UNC3334A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.46 (s, 1H), 8.22 (s, 1H), 7.74 (d, J = 1.6 Hz, 2H), 3.90- 3.79 (m, 1H), 3.68-3.51 (m, 3H), 3.47-3.37 (m, 1H), 2.39 (s,3H), 1.90-1.78 (m, 1H), 1.76-1.65 (m,3H), 1.63-1.37 (m, 14H); MS m/z 384.3 [M + H]⁺.

Example 21 UNC3096A General Procedure J:

Methyl 2-chloro-4-{[2-(2-hydroxyethoxy)ethyl]amino}pyrimidine-5-carboxylate

A solution of methyl 2,4-dichloropyrimidine-5-carboxylate (252 mg, 1.22 mmol) in i-PrOH (6 mL) was added 2-(2-aminoethoxy)ethanol (122 μL, 1.22 mmol) and DIEA (319 μL, 1.83 mmol) at 0° C. After 1.5 h the volatiles were removed under a reduced pressure and the residue was purified by ISCO silica gel column to provide the title compound (243 mg, 72%) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 8.67 (s, 1H), 3.90 (s, 3H), 3.82-3.74 (m, 4H), 3.70 (t, J=5.2 Hz, 2H), 3.67-3.61 (m, 2H), 2.17 (t, J=6.3 Hz, 1H).

Methyl 2-chloro-4-(8,8,9,9-tetramethyl-4,7-dioxa-1-aza-8-siladecan-1-yl)pyrimidine-5-carboxylate

A solution of methyl 2-chloro-4-{[2-(2-hydroxyethoxy)ethyl]amino}pyrimidine-5-carboxylate (99 mg, 0.36 mmol) in DMF (720 μL) was added imidazole (49 mg, 0.72 mmol) followed by TBDMSCl (60 mg, 0.396 mmol). The reaction mixture was stirred at room temperature for 1 h, diluted with H₂O (2 mL) and extracted with CH₂Cl₂ (3×2 mL). The combined organic layers were washed with brine (2×2 mL), dried (Na₂SO₄) and concentrated. The residue was purified by ISCO silica gel column to provide the title compound (137 mg, 98%) as a colorless oil.

Methyl 2-[(5-hydroxypentyl)amino]-4-(8,8,9,9-tetramethyl-4,7-dioxa-1-aza-8-siladecan-1-yl)pyrimidine-5-carboxylate

A solution of methyl 2-chloro-4-(8,8,9,9-tetramethyl-4,7-dioxa-1-aza-8-siladecan-1-yl)pyrimidine-5-carboxylate (133 mg, 0.341 mmol) in i-PrOH (3.4 mL) was added 5-aminopentan-1-ol (185 μL, 1.7 mmol) and DIEA (89 μL, 0.511 mmol). The reaction mixture was stirred at room temperature overnight. The solvents were removed under a reduced pressure and the residue was purified by ISCO silica gel column to provide the title compound (156 mg, >99%) as a colorless oil.

Methyl 5,8-dioxa-2,14,16,19-tetraazabicyclo[13.3.1]nonadeca-1(18),15(19),16-triene-18-carboxylate

A solution of methyl 2-[(5-hydroxypentyl)amino]-4-(8,8,9,9-tetramethyl-4,7-dioxa-1-aza-8-siladecan-1-yl)pyrimidine-5-carboxylate (150 mg, 0.328 mmol) in CH₂Cl₂ (3.3 mL) was added DIEA (143 μL, 0.82 mmol) then methane sulfonylchloride (28 μL, 0.361) at 0° C. The reaction mixture was stirred for 30 min and diluted with H₂O (12 mL). The organic layer was washed with brine (10 mL) and dried to provide the crude mesylate that was used for the next step without further purification. The mesylate was dissolved in THF (7.3 mL) and TBAF (1M in THF, 585 μL, 0.585 mmol) was added. The reaction mixture was stirred at room temperature overnight. The solvents were removed under a reduced pressure and the residue was purified by ISCO silica gel column to provide the title compound (32 mg, 34%) as a white solid. ¹H NMR (400 MHz, CDCl₃) δ 8.57 (s, 1H), 3.86-3.79 (m, 7H), 3.79-3.73 (m, 2H), 3.72-3.66 (m, 5H), 3.64-3.59 (m, 2H), 2.32 (dd, J=9.3, 3.6 Hz, 1H), 1.72-1.64 (m, 2H), 1.59 (dd, J=10.8, 5.7 Hz, 4H).

5,8-Dioxa-2,14,16,19-tetraazabicyclo[13.3.1]nonadeca-1(18),15(19),16-triene-18-carboxylic acid

A solution of methyl 5,8-dioxa-2,14,16,19-tetraazabicyclo[13.3.1]nonadeca-1(18),15(19),16-triene-18-carboxylate (32 mg, 0.099 mmol) in MeOH (1.4 mL) was added a 4.0 M KOH solution (250 μL). The reaction mixture was heated at 60° C. overnight. The reaction was cooled and the MeOH was removed under a reduced pressure. The mixture was acidified with a 4.0 N HCl solution to pH ˜2. The aqueous layer was extracted with 3:1 CH₂Cl₂/i-PrOH (3×5 mL). The combined organic layers were dried (Na₂SO₄) and concentrated to afford the title compound (35 mg, >99%) as a white solid.

N-{[6-(1H-Pyrazol-1-yl)pyridin-3-yl]methyl}-5,8-dioxa-2,14,16,19-tetraazabicyclo[13.3.1]nonadeca-1(18),15(19),16-triene-18-carboxamide (UNC3096A)

A solution of 5,8-dioxa-2,14,16,19-tetraazabicyclo[13.3.1]nonadeca-1(18),15(19),16-triene-18-carboxylic acid (30 mg, 0.099 mmol) in DMF (1.0 mL) was added [6-(1H-pyrazol-1-yl)pyridin-3-yl]methanamine (17 mg, 0.099 mmol) and DIEA (34 μL, 0.197 mmol) followed by HATU (41 mg, 0.108 mmol). The reaction mixture was stirred at room temperature overnight, quenched with a 1.0 M NaOH solution (2.0 mL) and extracted with CH₂Cl₂ (2×2 mL). The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was purified by HPLC to afford the title compound (37 mg, 67%) as a light yellow solid. ¹H NMR (400 MHz, CD₃OD) δ 8.62 (dd, J=2.7, 0.4 Hz, 1H), 8.50 (d, J=1.9 Hz, 1H), 8.32 (s, 1H), 8.15 (dd, J=8.6, 2.3 Hz, 1H), 8.03 (d, J=8.5 Hz, 1H), 7.85 (d, J=1.3 Hz, 1H), 6.61 (dd, J=2.7, 1.7 Hz, 1H), 4.59 (s, 2H), 3.85-3.63 (m, 10H), 3.63-3.55 (m, 2H), 1.81-1.65 (m, 6H). MS m/z 467.3 [M+H]⁺.

Table 21 describes compounds prepared following procedures described in Example 21 (General Procedure J), using appropriate reagents.

Physical Data Mer MS m/z (M + 1) Structure Compound_ID IC₅₀ or/and ¹H NMR 1

UNC2887A ++ ¹H NMR (400 MHz, CD₃OD) δ 8.59 (d, J = 2.6 Hz, 1H), 8.46 (d, J = 1.9 Hz, 1H), 8.26 (s, 1H), 8.03 (dd, J = 8.5, 2.3 Hz, 1H), 7.95 (d, J = 8.5 Hz, 1H), 7.79 (d, J = 1.4 Hz, 1H), 6.57 (dd, J = 2.6, 1.8 Hz, 1H), 4.57 (s, 2H), 3.85-3.71 (m, 6H), 3.69-3.64 (m, 2H), 3.64- 3.59 (m, 4H), 3.59-3.52 (m, 4H). MS m/z 469.3 [M + H]⁺.

Example 22 UNC3040A General Procedure K:

Ethyl 2,8,9,10,17,19,22-heptaazatricyclo[16.3.1.1⁷,¹⁰]tricosa-1(21),7(23),8,18(22),19-pentaene-21-carboxylate

A solution of 2,4-dichloropyrimidine-5-carbonyl chloride (1.00 g, 4.76 mmol) in ethanol (6.0 mL) was added DIPEA (2.5 mL, 14.4 mmol) slowly at 0° C. under nitrogen. After 30 min, hex-5-yn-1-amine (0.476 g, 4.91 mmol) was added in one portion. The reaction mixture was stirred at room temperature for 3.5 h, then was added dropwise to a solution of 6-azidohexan-1-amine (0.801 g, 5.64 mmol) in ethanol (4.0 mL) at 50° C. After the reaction was complete (monitored by LCMS), the mixture was diluted with water (10 mL) and concentrated under a reduced pressure and filtered. The yellow solid was washed with water and dried under vacuum to be used in the next step without further purification (0.723 g, 39% over 3 steps).

A solution of the yellow solid (0.130 g, 0.336 mmol) in dry CH₂Cl₂ (25 mL) was added TBTA (1.6 mL, 5 mg/mL in CH₂Cl₂, 8.0 mg, 0.016 mmol) and Cu(MeCN)₄BF₄ (5.2 mg, 0.016 mmol). The reaction mixture was stirred under nitrogen at 45° C. for 24 h, then cooled to room temperature and concentrate. The residue was purified by silica gel column to provide the title compound (0.104 g, 80%). ¹H NMR (400 MHz, CD₃OD) δ 8.34 (s, 2H), 7.58 (s, 1H), 4.36 (s, 2H), 4.22 (q, J=7.1 Hz, 2H), 3.34 (s, 2H), 3.19 (s, 2H), 2.82-2.66 (m, 2H), 1.84 (s, 2H), 1.67 (s, 2H), 1.62-1.44 (m, 4H), 1.40-1.02 (m, 7H).

2,8,9,10,17,19,22-Heptaazatricyclo[16.3.1.1⁷,¹⁰]tricosa-1(21),7(23),8,18(22),19-pentaene-21-carboxylic acid

A solution of ethyl 2,8,9,10,17,19,22-heptaazatricyclo[16.3.1.1⁷,¹⁰]tricosa-1(21),7(23),8,18(22),19-pentaene-21-carboxylate (31 mg, 0.081 mmol) in MeOH (2.0 mL) was added an aq. KOH solution (10%, 0.50 mL). The reaction was stirred at 60° C. for 12 h. Then the reaction mixture was cooled to room temperature and adjusted to pH=3 by the addition of a HCl solution. The resulting solution was extracted by a mixture of i-PrOH/CH₂Cl₂ (1:3, 10 mL×3). The combined organic layers were washed with water and brine and concentrated under vacuum to afford the desired product (0.029 g, quant.) as a white solid. ¹H NMR (400 MHz, CD₃OD) δ 8.41-8.22 (m, 1H), 5.65 (s, 2H), 4.63-4.46 (m, 1H), 3.55-3.43 (m, 1H), 3.39-3.33 (m, 1H), 3.02 (t, J=6.9 Hz, 3H), 2.97-2.83 (m, 1H), 2.58-2.29 (m, 3H), 2.03-1.89 (m, 1H), 1.85-1.71 (m, 1H), 1.71-1.50 (m, 2H), 1.49-0.97 (m, 3H).

N-(1-benzylpiperidin-41)-2,8,9,10,17,19,22-heptaazatricyclo[16.3.1.1⁷,¹⁰]tricosa-1(21),7(23),8,18(22),19-pentaene-21-carboxamid (UNC3040A)

A solution of 2,8,9,10,17,19,22-Heptaazatricyclo[16.3.1.1⁷,¹⁰]tricosa-1(21),7(23),8,18(22),19-pentaene-21-carboxylic acid (30 mg, 0.084 mmol) in DMF (2.0 mL) was added 1-benzylpiperidin-4-amine (19.8 mg, 0.10 mmol) followed by HATU (38 mg, 0.10 mmol). The reaction mixture was stirred at room temperature overnight, quenched with a 1.0 M NaOH solution (2.0 mL) and extracted with CH₂Cl₂ (2×2 mL) The combined organic layers were dried (Na₂SO₄) and concentrated. The residue was purified by HPLC to afford the title compound UNC3040A (6.0 mg, 13%) as a light yellow solid. ¹H NMR (400 MHz, CD₃OD) δ 8.24 (s, 1H), 8.08-7.93 (m, 2H), 7.64-7.46 (m, 4H), 4.54-4.46 (m, 2H), 4.33 (s, 1H), 3.59-3.40 (m, 4H), 3.22-3.05 (m, 2H), 3.02-2.93 (m, 3H), 2.91-2.77 (m, 3H), 2.37-2.26 (m, 1H), 2.25-2.13 (m, 2H), 1.98-1.86 (m, 3H), 1.79-1.70 (m, 2H), 1.66-1.50 (m, 4H), 1.30-1.10 (m, 4H); MS (ESI): 554.5 [M+Na]⁺.

Example 23 Trans-4-((2-(butylamino)-5-(5-((1-methylpiperidin-4-yl)methyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexan-1-ol (UNC4337A)

¹HNMR (400 MHz, CD₃OD) δ 8.51 (s, 1H), 8.29 (s, 1H), 7.88 (s, 2H), 4.19-4.07 (m, 1H), 3.70-3.62 (m, 1H), 3.55-3.40 (m, 4H), 3.02-2.93 (m, 2H), 2.84 (s, 3H), 2.72 (d, J=8.0 Hz, 2H), 2.20-2.12 (m, 2H), 2.05-1.96 (m, 2H), 1.96-1.89 (m, 3H), 1.71-1.62 (m, 2H), 1.62-1.38 (m, 8H), 1.00 (t, J=8.0 Hz, 3H). LC-MS (ESI+): t_(R)=4.484 min, MS m/z 453.0 [M+1]⁺.

Trans-4-((2-(butylamino)-5-(5-(1-isopropylpiperidin-4-ylidene)methyl)pyridine2yl)pyramidin-4-yl)amino)cyclohexan-1-ol (UNC4340A)

¹H NMR (400 MHz, CD₃OD) δ 8.53 (s, 1H), 8.34 (s, 1H), 7.90-7.83 (m, 2H), 6.56 (s, 1H), 4.20-4.05 (m, 1H), 3.70-3.58 (m, 2H), 3.58-3.45 (m, 3H), 3.19-3.00 (m, 3H), 2.90-2.60 (m, 3H), 2.19-2.11 (m, 2H), 2.05-1.96 (m, 2H), 1.71-1.63 (m, 2H), 1.60-1.40 (m, 6H), 1.39 (d, J=8.0 Hz, 3H), 1.00 (t, J=8.0 Hz, 3H). LC-MS (ESI+): t_(R)=4.556 min, MS m/z 479.0 [M+1]⁺.

Trans-4-((5-(pyridin-2-yl)-2-(pyridin-3-ylamino)pyrimidin-4-yl)amino)cyclohexan-1-ol (UNC3209A)

¹H NMR (400 MHz, CD₃OD) δ 9.35 (d, J=2.0 Hz, 1H), 8.88 (d, J=2.0 Hz, 1H), 8.76-8.73 (m, 2H), 8.56 (s, 1H), 8.23-8.13 (s, 2H), 8.11 (d, J=8.0 Hz, 1H), 7.68-7.65 (m, 1H), 4.13-4.07 (m, 1H), 3.70-3.64 (m, 1H), 2.16-2.12 (m, 2H), 2.04-2.00 (m, 2H), 1.58-1.44 (m, 4H). LC-MS (ESI+): t_(R)=4.690 min, MS m/z 363.0 [M+1]⁺.

5-(2-(Butylamino)-4-((trans-4-hydroxycyclohexyl)amino)pyrimidin-5-yl)furan-2-carbaldehyde (UNC2902A)

¹H NMR (400 MHz, cdcl₃) δ 9.49 (s, 1H), 8.22 (s, 1H), 7.28 (d, J=3.8 Hz, 1H), 6.55 (d, J=3.8 Hz, 1H), 5.25-5.07 (m, 1H), 4.13-3.98 (m, 1H), 3.79-3.70 (m, 1H), 3.41 (dd, J=13.3, 6.9 Hz, 2H), 2.25-2.15 (m, 2H), 2.10-2.01 (m, 2H), 1.79-1.68 (m, 1H), 1.65-1.55 (m, 2H), 1.54-1.34 (m, 5H), 0.95 (t, J=7.3 Hz, 3H); ¹³C NMR (101 MHz, cdcl₃) δ 175.1, 161.9, 158.9, 157.7, 156.1, 150.4, 125.0, 104.4, 69.6, 48.6, 41.2, 33.6, 31.9, 30.2, 20.1, 13.9; MS m/z 359.20 [M+H]⁺.

Example 24 MerTK, Axl, Tyro3, and Flt3 Kinase Activity of Active Compounds

Inhibition constants of MerTK, Flt3, Tyro3 and Axl kinase activity by an active compound as described herein is determined at the Km for ATP using a microfluidic capillary electrophoresis (MCE) assay in which phosphorylated and unphosphorylated substrate peptides were separated and analyzed using a LabChip EZ Reader. See, Liu J, et al. UNC1062, a new and potent MerTK inhibitor. Eur J Med Chem. 2013; 65:83-93; Liu J, et al. Discovery of novel small molecule MerTK kinase inhibitors for the treatment of pediatric acute lymphoblastic leukemia. ACS Med Chem Lett. 2012; 3:129-134; Pommereau A, Pap E, Kannt A. Two simple and generic antibody-independent kinase assays: comparison of a bioluminescent and a microfluidic assay format. J Biomol Screen. 2004; 9: 409-416; Dunne J, Reardon H, Trinh V, Li E, Farinas J. Comparison of on-chip and off-chip microfluidic kinase assay formats. Assay Drug Dev Technol. 2004; 2:121-129; Bernasconi P, Chen M, Galasinski S, Popa-Burke I, Bobasheva A, Coudurier L, Birkos S, Hallam R, Janzen W P. A chemogenomic analysis of the human proteome: application to enzyme families. J Biomol Screen. 2007; 12:972-982.

Briefly, activity assays were performed in a 384 well, polypropylene microplate in a final volume of 50 μL of 50 mM Hepes, Ph 7.4 containing 10 mM MgCl₂, 1.0 mM DTT, 0.01% Triton X-100, 0.1% Bovine Serum Albumin (BSA), containing 1.0 μM fluorescent substrate and ATP at the Km for each enzyme. All reactions were terminated by addition of 20 μL of 70 mM EDTA. After a 180 min incubation, phosphorylated and unphosphorylated substrate peptides were separated in buffer supplemented with 1×CR-8 on a LabChip EZ Reader equipped with a 12-sipper chip. Data were analyzed using EZ Reader software. Assay conditions for MCE assays

Kinase Kinase Peptide Substrate (nM) ATP (uM) Mer 5-FAM-EFPIYDFLPAKKK-CONH₂ 2.0 5.0 Axl 5-FAM-KKKKEEIYFFF-CONH₂ 120 65 Tyro 5-FAM-EFPIYDFLPAKKK-CONH₂ 10 21

TABLE 22 MERTK, AXL, TYRO3, AND FLT3 KINASE ACTIVITY OF SELECT PYRIMIDINE COMPOUNDS Compound_ID IC₅₀ Data (nM) UNC1844A IC₅₀ MerTK 14 nM nM Tyro3 1083 nM nM Axl 1179 UNC1845A IC₅₀ MerTK 15 nM nM Tyro3 1029 nM nM Axl 1159 UNC1846A IC₅₀ MerTK 27 nM Tyro3 1068 nM Axl 1185 nM UNC1849A IC₅₀ MerTK 8.7 nM Tyro3 1743 nM Axl 1263 nM UNC1850A IC₅₀ MerTK 21 nM Tyro3 1215 nM Axl 1643 nM UNC1839A IC₅₀ MerTK 8.6 nM Tyro3 1073 nM Axl 951 nM UNC1840A IC₅₀ MerTK 211 nM Tyro3 4637 nM Axl 5542 nM UNC2579A Flt3 137 nM IC₅₀ MerTK 13 nM Tyro3 381 nM Axl 1516 nM UNC2580A Flt3 108 nM IC₅₀ MerTK 5.8 nM Tyro3 233 nM Axl 512 nM UNC2581A Flt3 181 nM IC₅₀ MerTK 9.6 nM Tyro3 643 nM Axl 698 nM UNC2582A Flt3 407 nM IC₅₀ MerTK 17 nM Tyro3 436 nM Axl 1397 nM UNC2583A Flt3 190 nM IC₅₀ MerTK 16 nM Tyro3 527 nM Axl 1797 nM UNC2591A Tyro3 1508 nM Flt3 536 nM Axl 2038 nM IC₅₀ MerTK 29 nM UNC2592A Tyro3 285 nM Flt3 57 nM IC₅₀ MerTK 9.1 nM Axl 4947 nM UNC2584A Flt3 101 nM IC₅₀ MerTK 4.5 nM Tyro3 273 nM Axl 1124 nM UNC2585A Flt3 585 nM IC₅₀ MerTK 21 nM Tyro3 1102 nM Axl 2818 nM UNC2593A Tyro3 559 nM Flt3 183 nM IC₅₀ MerTK 23 nM Axl 683 nM UNC2587A Flt3 101 nM IC₅₀ MerTK 8.8 nM Tyro3 291 nM Axl 632 nM UNC2586A Flt3 146 nM IC₅₀ MerTK 7.7 nM Tyro3 477 nM Axl 1098 nM UNC2594A Tyro3 118 nM Flt3 48 nM Axl 221 nM IC₅₀ MerTK 2.6 nM UNC2595A Flt3 74 nM Axl 422 nM Tyro3 215 nM IC₅₀ MerTK 8.2 nM UNC2598A Tyro3 214 nM IC₅₀ MerTK 1.6 nM Flt3 42 nM Axl 427 nM UNC2599A Tyro3 165 nM Flt3 48 nM Axl 241 nM IC₅₀ MerTK 3.1 nM UNC2600A Tyro3 159 nM Flt3 86 nM Axl 196 nM IC₅₀ MerTK 4.5 nM UNC2601A Tyro3 249 nM Flt3 220 nM Axl 618 nM IC₅₀ MerTK 12 nM UNC2602A Tyro3 371 nM Flt3 37 nM Axl 368 nM IC₅₀ MerTK 8.3 nM UNC2603A Tyro3 506 nM Flt3 362 nM Axl 1116 nM IC₅₀ MerTK 19 nM UNC2604A Tyro3 412 nM Flt3 120 nM IC₅₀ MerTK 19 nM Axl 1198 nM UNC2605A Tyro3 240 nM Flt3 105 nM Axl 684 nM IC₅₀ MerTK 9.4 nM UNC2627A Axl 1661 nM Flt3 32 nM Tyro3 833 nM IC₅₀ MerTK 29 nM UNC2628A Axl 566 nM Flt3 7.8 nM Tyro3 448 nM IC₅₀ MerTK 13 nM UNC2629A Tyro3 241 nM Axl 366 nM Flt3 2.8 nM IC₅₀ MerTK 6.7 nM UNC2694A Tyro3 483 nM IC₅₀ MerTK 4.2 nM Axl 557 nM Flt3 62 nM UNC2695A Tyro3 76 nM IC₅₀ MerTK 4.3 nM Axl 233 nM Flt3 45 nM UNC2696A Tyro3 191 nM IC₅₀ MerTK 8.3 nM Axl 430 nM Flt3 226 nM UNC2697A IC₅₀ MerTK 18 nM Axl 999 nM Tyro3 217 nM Flt3 94 nM UNC2698A Tyro3 43 nM IC₅₀ MerTK 5.3 nM Axl 175 nM Flt3 77 nM UNC2732A Tyro3 539 nM Flt3 113 nM IC₅₀ MerTK 12 nM Axl 575 nM UNC2733A Tyro3 366 nM Flt3 50 nM IC₅₀ MerTK 12 nM Axl 427 nM UNC2734A Tyro3 505 nM Flt3 30 nM IC₅₀ MerTK 12 nM Axl 665 nM UNC2735A Tyro3 145 nM Flt3 58 nM IC₅₀ MerTK 4.1 nM Axl 189 nM UNC2736A Tyro3 384 nM Flt3 12 nM IC₅₀ MerTK 8 nM Axl 465 nM UNC2737A Flt3 19 nM IC₅₀ MerTK 12 nM Tyro3 443 nM Axl 491 nM UNC2742A Tyro3 247 nM IC₅₀ MerTK 22 nM Flt3 138 nM Axl 534 nM UNC2743A Tyro3 84 nM IC₅₀ MerTK 5 nM Flt3 61 nM Axl 166 nM UNC2744A Tyro3 172 nM IC₅₀ MerTK 2.6 nM Flt3 70 nM Axl 277 nM UNC2761A Tyro3 208 nM IC₅₀ MerTK 7.6 nM Flt3 79 nM Axl 319 nM UNC2762A Tyro3 148 nM IC₅₀ MerTK 4.5 nM Flt3 37 nM Axl 220 nM UNC2763A Tyro3 502 nM IC₅₀ MerTK 35 nM Flt3 237 nM Axl 1092 nM UNC2799A IC₅₀ MerTK 281 nM Flt3 135 nM Tyro3 30000 nM Axl 30000 nM UNC2764A Tyro3 115 nM IC₅₀ MerTK 8.6 nM Flt3 2.5 nM Axl 177 nM UNC2775A IC₅₀ MerTK 39 nM Flt3 501 nM Tyro3 1474 nM Axl 3811 nM UNC2776A IC₅₀ MerTK 15 nM Flt3 11 nM Tyro3 658 nM Axl 880 nM UNC2800A IC₅₀ MerTK 5.3 nM Flt3 58 nM Tyro3 130 nM Axl 314 nM UNC2801A IC₅₀ MerTK 3.2 nM Flt3 60 nM Tyro3 113 nM Axl 205 nM UNC2802A IC₅₀ MerTK 4.3 nM Flt3 105 nM Tyro3 123 nM Axl 408 nM UNC2803A IC₅₀ MerTK 247 nM Flt3 94 nM Tyro3 21952 nM Axl 21075 nM UNC2804A IC₅₀ MerTK 7 nM Flt3 121 nM Tyro3 210 nM Axl 592 nM UNC2805A IC₅₀ MerTK 8.8 nM Flt3 3.4 nM Tyro3 184 nM Axl 409 nM UNC2806A IC₅₀ MerTK 7.2 nM Flt3 2.2 nM Tyro3 98 nM Axl 266 nM UNC2876A Tyro3 150 nM Flt3 49 nM IC₅₀ MerTK 3.6 nM Axl 218 nM UNC2877A Tyro3 230 nM Flt3 70 nM IC₅₀ MerTK 4 nM Axl 245 nM UNC2878A Tyro3 166 nM Flt3 84 nM IC₅₀ MerTK 4.2 nM Axl 191 nM UNC2879A Tyro3 280 nM Flt3 93 nM IC₅₀ MerTK 5.6 nM Axl 342 nM UNC2880A Tyro3 559 nM Flt3 197 nM IC₅₀ MerTK 7.4 nM Axl 812 UNC2881A Tyro3 254 nM Flt3 55 nM IC₅₀ MerTK 4.3 nM Axl 563 nM UNC2886A IC₅₀ MerTK 4.8 nM Tyro3 183 nM Flt3 34 nM Axl 325 UNC2918A IC₅₀ MerTK 4.5 nM Tyro3 145 nM Flt3 95 nM Axl 667 nM UNC2956A Axl 136 nM Flt3 15 nM IC₅₀ MerTK 3.2 nM Tyro3 200 nM UNC2969A Axl 667 nM Flt3 143 nM IC₅₀ MerTK 14 nM Tyro3 1061 nM UNC2957A Axl 593 nM Flt3 155 nM IC₅₀ MerTK 14 nM Tyro3 975 UNC3004A Axl 822 nM Flt3 89 nM IC₅₀ MerTK 4.6 nM Tyro3 272 nM UNC3111A IC₅₀ MerTK 40 nM Tyro3 2162 nM Flt3 592 nM Axl 5040 nM UNC3112A IC₅₀ MerTK 77 nM Tyro3 5150 nM Flt3 1477 nM Axl 30000 nM UNC3144A IC₅₀ MerTK 2.5 nM Tyro3 360 nM Axl 487 nM Flt3 46 nM UNC3145A IC₅₀ MerTK 17 nM Tyro3 631 nM Axl 1101 nM Flt3 48 nM UNC3183A Flt3 60 nM Axl 703 nM IC₅₀ MerTK 7.2 nM Tyro3 372 nM UNC4234A IC₅₀ MerTK 5.8 nM Axl 470 nM Flt3 41 nM Tyro3 195 nM UNC4235A IC₅₀ MerTK 80 nM Axl 1800 nM 385 nM Tyro3 1271 nM UNC4236A IC₅₀ MerTK 3.8 nM Axl 216 nM Flt3 31 nM Tyro3 92 nM UNC4238A IC₅₀ MerTK 26 nM Axl 698 nM Flt3 133 nM Tyro3 242 nM UNC4239A IC₅₀ MerTK 14 nM Axl 977 nM Flt3 87 nM Tyro3 305 nM UNC4246A IC₅₀ MerTK 4.6 nM Axl 489 nM Flt3 58 nM Tyro3 244 nM UNC4254A IC₅₀ MerTK 39 nM Tyro3 375 nM Axl 716 nM Flt3 185 nM UNC4255A IC₅₀ MerTK 4 nM Tyro3 156 nM Axl 336 nM Flt3 76 nM UNC4256A IC₅₀ MerTK 9 nM Tyro3 340 nM Axl 743 nM Flt3 124 nM UNC4260A IC₅₀ MerTK 4.8 nM Tyro3 256 nM Axl 602 nM Flt3 77 nM UNC4274A IC₅₀ MerTK 20 nM Tyro3 1063 nM Axl 2018 nM Flt3 742 nM UNC4286A IC₅₀ MerTK 20 nM Axl 572 nM Tyro3 253 nM Flt3 44 nM UNC4285A IC₅₀ MerTK 8.1 nM Tyro3 311 nM Axl 555 nM Flt3 94 nM UNC4287A IC₅₀ MerTK 38 nM Axl 960 nM Tyro3 494 nM Flt3 204 nM UNC4288A IC₅₀ MerTK 6.8 nM Axl 1052 nM Tyro3 262 nM Flt3 114 nM UNC4289A IC₅₀ MerTK 11 nM Axl 420 nM Tyro3 178 nM Flt3 83 nM UNC4290A IC₅₀ MerTK 34 nM Axl 656 nM Tyro3 375 nM Flt3 278 nM UNC4302A Tyro3 153 nM Axl 292 nM IC₅₀ MerTK 9.7 nM Flt3 123 nM UNC4303A Axl 777 nM IC₅₀ MerTK 77 nM Tyro3 486 nM Flt3 295 nM UNC4304A Axl 664 nM IC₅₀ MerTK 3.8 nM Tyro3 333 nM Flt3 130 nM UNC4307A Axl 471 nM IC₅₀ MerTK 9.3 nM Tyro3 217 nM Flt3 142 nM UNC4344A Flt3 55 nM IC₅₀ MerTK 2.9 nM Tyro3 276 nM Axl 196 nM UNC3055A Axl 8704 nM Flt3 16 nM IC₅₀ MerTK 18 nM Tyro3 313 nM UNC2794A IC₅₀ MerTK 14 nM Flt3 56 nM Tyro3 158 nM Axl 604 nM UNC2860A Tyro3 755 nM Flt3 13 nM IC₅₀ MerTK 13 nM Axl 30000 nM UNC2863A Tyro3 1216 nM Flt3 74 nM IC₅₀ MerTK 16 nM Axl 2614 nM UNC2250B IC₅₀ MerTK 1.8 nM Tyro3 104 nM Axl 271 nM Flt3 10 nM UNC2432A IC₅₀ MerTK 0.69 nM Tyro3 24 nM Axl 44 nM Flt3 2.6 nM UNC2422A IC₅₀ MerTK 1.1 nM Tyro3 36 nM Axl 129 nM Flt3 7.8 nM UNC3021A Axl 621 nM Flt3 4.2 nM IC₅₀ MerTK 9.6 nM Tyro3 114 nM UNC2405A IC₅₀ MerTK 5 nM Tyro3 98 nM Axl 183 nM Flt3 13 nM UNC2490A IC₅₀ MerTK 1.5 nM Tyro3 18 nM Axl 36 nM Flt3 4.7 nM UNC2550A IC₅₀ MerTK 0.49 nM Flt3 2.1 nM Axl 39 nM Tyro3 13 nM UNC2491A IC₅₀ MerTK 1.3 nM Tyro3 32 nM Axl 84 nM Flt3 5.2 nM UNC2489A IC₅₀ MerTK 0.63 nM Tyro3 16 nM Axl 34 nM Flt3 2.2 nM UNC2547A IC₅₀ MerTK 0.56 nM Flt3 3.5 nM Axl 30 nM Tyro3 11 nM UNC2488A IC₅₀ MerTK 1.7 nM Tyro3 21 nM Axl 62 nM Flt3 7 nM UNC2549A IC₅₀ MerTK 1.2 nM Flt3 4.9 nM Axl 66 nM Tyro3 18 nM UNC2546A IC₅₀ MerTK 0.81 nM Flt3 3.8 nM Axl 69 nM Tyro3 20 nM UNC2571A Flt3 3.2 nM IC₅₀ MerTK 0.47 nM Tyro3 18 nM Axl 44 nM UNC2572A Flt3 8.9 nM IC₅₀ MerTK 0.76 nM Tyro3 43 nM Axl 136 nM UNC2621A Tyro3 70 nM Axl 221 nM Flt3 11 nM IC₅₀ MerTK 5 nM UNC2622A Tyro3 162 nM Axl 296 nM Flt3 13 nM IC₅₀ MerTK 12 nM UNC2252A IC₅₀ MerTK 1.3 nM Tyro3 42 nM Flt3 4.4 nM Axl 120 nM UNC2251B IC₅₀ MerTK 0.84 nM Tyro3 24 nM Axl 95 nM Flt3 5.2 nM UNC3125A IC₅₀ MerTK 19 nM Tyro3 259 nM Flt3 26 nM Axl 1130 nM UNC2862A Tyro3 88 nM Flt3 6 nM IC₅₀ MerTK 2.8 nM Axl 216 nM UNC2606A Tyro3 24 nM Flt3 2.9 nM IC₅₀ MerTK 0.69 nM Axl 61 nM UNC3027A Axl 125 nM Flt3 8.6 nM IC₅₀ MerTK 1 nM Tyro3 31 nM UNC2915A IC₅₀ MerTK 2.2 nM Tyro3 6.5 nM Flt3 5.1 nM Axl 49 nM UNC3056A Axl 30000 nM Flt3 29 nM IC₅₀ MerTK 6.9 nM Tyro3 152 UNC2795A IC₅₀ MerTK 14 nM Flt3 27 nM Tyro3 82 nM Axl 211 nM UNC2793A IC₅₀ MerTK 7.1 nM Flt3 20 nM Tyro3 60 nM Axl 153 nM UNC2792A IC₅₀ MerTK 9.2 nM Flt3 18 nM Tyro3 75 nM Axl 191 nM UNC2777A IC₅₀ MerTK 3.4 nM Flt3 11 nM Tyro3 94 nM Axl 167 nM UNC2710A IC₅₀ MerTK 12 nM Axl 992 nM Tyro3 421 nM Flt3 41 nM UNC2711A IC₅₀ MerTK 6 nM Tyro3 265 nM Axl 644 nM Flt3 26 nM UNC2790A IC₅₀ MerTK 12 nM Flt3 45 nM Tyro3 338 nM Axl 835 nM UNC2791A IC₅₀ MerTK 9.5 nM Flt3 41 nM Tyro3 416 nM Axl 886 nM UNC2713A IC₅₀ MerTK 5.4 nM Axl 522 nM Tyro3 325 nM Flt3 41 nM UNC2712A Tyro3 209 nM IC₅₀ MerTK 5.3 nM Axl 364 nM Flt3 39 nM UNC2898A IC₅₀ MerTK 39 nM Tyro3 374 nM Flt3 51 nM Axl 2551 nM UNC2899A IC₅₀ MerTK 50 nM Tyro3 414 nM Flt3 40 nM Axl 2261 nM UNC2900A IC₅₀ MerTK 32 nM Tyro3 370 nM Flt3 19 nM Axl 1850 nM UNC2902A IC₅₀ MerTK 34 nM Tyro3 241 nM Flt3 62 nM Axl 1632 nM UNC3181A Flt3 131 nM Axl 1027 nM IC₅₀ MerTK 33 nM Tyro3 507 nM UNC4103A IC₅₀ MerTK 0.43 nM Tyro3 1.3 nM Flt3 0.42 nM Axl 4.4 nM UNC4104A IC₅₀ MerTK 1 nM Tyro3 11 nM Flt3 5.5 nM UNC4161A IC₅₀ MerTK 1.5 nM Tyro3 7.7 nM Axl 16 nM Flt3 6.6 nM UNC4162A IC₅₀ MerTK 0.83 nM Tyro3 5.2 nM Axl 17 nM Flt3 2.6 nM UNC4163A IC₅₀ MerTK 1.2 nM Tyro3 8.7 nM Axl 20 nM Flt3 3 nM UNC4165A IC₅₀ MerTK 1.5 nM Tyro3 8 nM Axl 18 nM Flt3 2.8 nM UNC4197A IC₅₀ MerTK 6.6 nM Tyro3 24 nM Axl 43 nM Flt3 12 nM UNC3668A IC₅₀ MerTK 167 nM Axl 5300 nM Tyro3 409 nM Flt3 9422 nM UNC2958A Axl 180 nM Flt3 4.6 nM IC₅₀ MerTK 4.5 nM Tyro3 58 nM UNC2960A Axl 19943 nM Flt3 717 nM IC₅₀ MerTK 1126 nM Tyro3 4910 nM UNC2964A Axl 5266 nM Flt3 211 nM IC₅₀ MerTK 385 nM Tyro3 2772 nM UNC3003A Axl 30000 nM Flt3 30000 nM IC₅₀ MerTK 20000 nM Tyro3 30000 nM UNC2961A Axl 3089 nM Flt3 34 nM IC₅₀ MerTK 34 nM Tyro3 433 UNC2962A Axl 2799 nM Flt3 39 nM IC₅₀ MerTK 72 nM Tyro3 385 nM UNC2996A Axl 19187 nM Flt3 547 nM IC₅₀ MerTK 598 nM Tyro3 4065 nM UNC2997A Axl 30000 nM Flt3 3760 nM IC₅₀ MerTK 2403 nM Tyro3 20045 nM UNC2998A Axl 30000 nM Flt3 19 nM IC₅₀ MerTK 21 nM Tyro3 363 nM UNC3000A Axl 1453 nM Flt3 50 nM IC₅₀ MerTK 17 nM Tyro3 282 nM UNC2999A Axl 596 nM Flt3 6.7 nM IC₅₀ MerTK 1.8 nM Tyro3 84 nM UNC3001A Axl 675 nM Flt3 3.9 nM IC₅₀ MerTK 18 nM Tyro3 169 nM UNC2959A Axl 30000 nM Flt3 1015 nM IC₅₀ MerTK 1251 nM Tyro3 30000 nM UNC3002A Axl 3698 nM Flt3 231 nM IC₅₀ MerTK 164 nM Tyro3 1374 nM UNC3014A Axl 30000 nM Flt3 30000 nM IC₅₀ MerTK 30000 nM Tyro3 30000 nM UNC3041A Axl 968 nM Flt3 56 nM IC₅₀ MerTK 13 nM Tyro3 605 nM UNC3042A Axl 558 nM Flt3 44 nM IC₅₀ MerTK 6.2 nM Tyro3 192 nM UNC3043A Axl 2306 nM Flt3 89 nM IC₅₀ MerTK 64 nM Tyro3 1638 nM UNC3044A Axl 912 nM Flt3 21 nM IC₅₀ MerTK 9.5 nM Tyro3 377 nM UNC3045A Axl 835 nM Flt3 89 nM IC₅₀ MerTK 25 nM Tyro3 529 nM UNC3046A Axl 160 nM Flt3 8.7 nM IC₅₀ MerTK 3.9 nM Tyro3 110 nM UNC3047A Axl 597 nM Flt3 11 nM IC₅₀ MerTK 4.9 nM Tyro3 157 nM UNC3048A Axl 400 nM Flt3 32 nM IC₅₀ MerTK 7.3 nM Tyro3 229 nM UNC3049A Axl 4436 nM Flt3 39 nM IC₅₀ MerTK 7.2 nM Tyro3 221 nM UNC3069A Axl 419 nM Flt3 11 nM IC₅₀ MerTK 5 nM Tyro3 176 nM UNC3071A Axl 275 nM Flt3 20 nM IC₅₀ MerTK 8.8 nM Tyro3 298 nM UNC3072A Axl 123 nM Flt3 3.8 nM IC₅₀ MerTK 1.2 nM Tyro3 43 nM UNC3074A Axl 754 nM Flt3 30 nM IC₅₀ MerTK 6.5 nM Tyro3 255 nM UNC3126A IC₅₀ MerTK 2 nM Tyro3 109 nM Flt3 3.1 nM Axl 364 nM UNC3113A IC₅₀ MerTK 2.4 nM Tyro3 77 nM Flt3 3.2 nM Axl 255 nM UNC3114A IC₅₀ MerTK 5 nM Tyro3 237 nM Flt3 5.4 nM Axl 791 nM UNC3115A IC₅₀ MerTK 4.1 nM Tyro3 415 nM Flt3 9.8 nM Axl 642 nM UNC3116A IC₅₀ MerTK 91 nM Tyro3 3939 nM Flt3 124 nM Axl 10018 nM UNC3117A IC₅₀ MerTK 977 nM Tyro3 30000 nM Flt3 1334 nM Axl 30000 nM UNC3118A IC₅₀ MerTK 1.1 nM Tyro3 23 nM Flt3 2.7 nM Axl 113 nM UNC3119A IC₅₀ MerTK 336 nM Tyro3 9625 nM Flt3 2656 nM Axl 30000 nM UNC3120A IC₅₀ MerTK 4 nM Tyro3 130 nM Flt3 5.8 nM Axl 315 nM UNC3130A IC₅₀ MerTK 15 nM Tyro3 384 nM Flt3 5.2 nM Axl 1087 nM UNC3121A IC₅₀ MerTK 1.7 nM Tyro3 71 nM Flt3 2.8 nM Axl 96 nM UNC3134A IC₅₀ MerTK 2.3 nM Tyro3 62 nM Axl 146 nM Flt3 4.9 UNC3135A IC₅₀ MerTK 6.3 nM Tyro3 165 nM Axl 304 nM Flt3 8.6 nM UNC3136A IC₅₀ MerTK 4.5 nM Tyro3 76 nM Axl 237 nM Flt3 3.1 nM UNC3137A IC₅₀ MerTK 34 nM Tyro3 412 nM Axl 1234 nM Flt3 21 nM UNC3138A IC₅₀ MerTK 31 nM Tyro3 935 nM Axl 1253 nM Flt3 38 UNC3139A IC₅₀ MerTK 290 nM Tyro3 2546 nM Axl 4542 nM Flt3 313 nM UNC3140A IC₅₀ MerTK 6.9 nM Tyro3 322 nM Axl 395 nM Flt3 6.9 nM UNC3141A IC₅₀ MerTK 8.6 nM Axl 30000 nM Flt3 32 nM UNC3146A IC₅₀ MerTK 19 nM Tyro3 1009 nM Axl 984 nM Flt3 31 nM UNC3149A IC₅₀ MerTK 26 nM Tyro3 30000 nM Axl 30000 nM Flt3 74 nM UNC3182A Flt3 4914 nM Axl 30000 nM IC₅₀ MerTK 1715 nM Tyro3 30000 nM UNC3331A IC₅₀ MerTK 8.4 nM Flt3 76 nM Tyro3 95 nM Axl 414 nM UNC3201A Flt3 6.3 nM Axl 112 nM IC₅₀ MerTK 1.7 nM Tyro3 195 nM UNC3191A Flt3 4 nM Axl 179 nM IC₅₀ MerTK 2.3 nM Tyro3 139 nM UNC3192A Flt3 1.3 nM Axl 86 nM IC₅₀ MerTK 1.3 nM Tyro3 77 nM UNC3200A Flt3 2.3 nM Axl 480 nM IC₅₀ MerTK 4.6 nM Tyro3 259 nM UNC3190A Flt3 2.9 nM Axl 135 nM IC₅₀ MerTK 2.5 nM Tyro3 90 nM UNC3193A Flt3 4.7 nM Axl 169 nM IC₅₀ MerTK 3.2 nM Tyro3 115 nM UNC3195A Flt3 4.1 nM Axl 188 nM IC₅₀ MerTK 2.8 nM Tyro3 230 nM UNC3194A Flt3 2.2 nM Axl 260 nM IC₅₀ MerTK 1.7 nM Tyro3 239 nM UNC3199A Flt3 5.6 nM Axl 1356 nM IC₅₀ MerTK 34 nM Tyro3 847 nM UNC3198A Flt3 24 nM Axl 6073 nM IC₅₀ MerTK 85 nM Tyro3 3736 nM UNC3196A Flt3 5.5 nM Axl 2128 nM IC₅₀ MerTK 26 nM Tyro3 1003 nM UNC3197A Flt3 7.7 nM Axl 1681 nM IC₅₀ MerTK 41 nM Tyro3 1174 nM UNC3203A Flt3 2 nM Axl 39 nM IC₅₀ MerTK 2.3 nM Tyro3 3.7 nM UNC4223A IC₅₀ MerTK 2.3 nM Tyro3 14 nM Axl 29 nM Flt3 3 nM UNC4261A IC₅₀ MerTK 6.7 nM Tyro3 380 nM Axl 579 nM Flt3 14 nM UNC4268A IC₅₀ MerTK 3.1 nM Tyro3 82 nM Axl 245 nM Flt3 5.5 nM UNC4269A IC₅₀ MerTK 12 nM Tyro3 234 nM Axl 513 nM Flt3 19 nM UNC4270A IC₅₀ MerTK 2.9 nM Tyro3 121 nM Axl 158 nM Flt3 10 nM UNC4272A IC₅₀ MerTK 14 nM Tyro3 194 nM Axl 12326 nM Flt3 32 nM UNC4322A Tyro3 889 nM Axl 30000 nM IC₅₀ MerTK 19 nM Flt3 76 nM UNC4323A Axl 30000 nM IC₅₀ MerTK 17 nM Tyro3 619 nM Flt3 150 nM UNC4333A Axl 30000 nM IC₅₀ MerTK 7.8 nM Tyro3 867 nM Flt3 160 nM UNC4353A Flt3 554 nM IC₅₀ MerTK 3.7 nM Tyro3 15142 nM Axl 30000 nM UNC3664A IC₅₀ MerTK 1.2 nM Axl 93 nM Tyro3 18 nM Flt3 3 nM UNC3665A IC₅₀ MerTK 771 nM Axl 30000 nM Tyro3 3074 nM Flt3 30000 nM UNC3666A IC₅₀ MerTK 0.94 nM Axl 52 nM Tyro3 11 nM Flt3 1.6 nM UNC3667A IC₅₀ MerTK 0.61 nM Axl 47 nM Tyro3 7.4 nM Flt3 1 nM UNC3669A IC₅₀ MerTK 2 nM Axl 26 nM Tyro3 7.7 nM Flt3 7.2 nM UNC4359A Flt3 32 nM IC₅₀ MerTK 7.2 nM Tyro3 568 nM Axl 435 nM UNC3022A Axl 760 nM Flt3 76 nM IC₅₀ MerTK 19 nM Tyro3 442 nM UNC3051A Axl 30000 nM Flt3 1366 nM IC₅₀ MerTK 376 nM Tyro3 30000 nM UNC3053A Axl 20251 nM Flt3 1321 nM IC₅₀ MerTK 82 nM Tyro3 1164 nM UNC3052A Axl 30000 nM Flt3 30000 nM IC₅₀ MerTK 16490 nM Tyro3 30000 nM UNC3204A Flt3 9.6 nM Axl 147 nM IC₅₀ MerTK 16 nM Tyro3 32 UNC3223A Flt3 8.5 nM Axl 164 nM IC₅₀ MerTK 5.3 nM Tyro3 2.6 nM UNC3206A Flt3 9003 nM Axl 30000 nM IC₅₀ MerTK 17982 nM Tyro3 15135 nM UNC3207A Flt3 21 nM Axl 256 nM IC₅₀ MerTK 31 nM Tyro3 38 nM UNC3205A Flt3 30000 nM Axl 30000 nM IC₅₀ MerTK 30000 nM Tyro3 50 nM UNC3224A Flt3 95 nM Axl 30000 nM IC₅₀ MerTK 154 nM Tyro3 81 nM UNC3209A Flt3 14 nM Axl 285 nM IC₅₀ MerTK 9.1000 nM Tyro3 14 nM UNC3208A Flt3 1.5 nM Axl 77 nM IC₅₀ MerTK 3.2 nM Tyro3 5.1 nM UNC4240A IC₅₀ MerTK 2.8 nM Axl 11 nM Flt3 2.6 nM Tyro3 2.4 UNC4241A IC₅₀ MerTK 1.3 nM Axl 6.8 nM Flt3 1.1 nM Tyro3 1.5 nM UNC4242A IC₅₀ MerTK l nM Axl 6.7 nM Flt3 1.5 nM Tyro3 1.2 UNC4243A IC₅₀ MerTK 4.6 nM Tyro3 3.8 nM Axl 13 nM Flt3 6.3 nM UNC4244A IC₅₀ MerTK 3.5 nM Axl 93 nM Flt3 12 nM Tyro3 3.2 nM UNC4247A IC₅₀ MerTK 1.7 nM Axl 7.9 nM Flt3 2.3 nM Tyro3 1.3 UNC4372A IC₅₀ MerTK 1.3 nM Tyro3 3.6 nM Axl 3.9 nM Flt3 0.96 nM UNC4373A IC₅₀ MerTK 1.6 nM Tyro3 4.5 nM Axl 2.7 nM Flt3 1.4 nM UNC4377A IC₅₀ MerTK 1.7 nM Tyro3 4.6 nM Axl 2.8 nM Flt3 1.3 nM UNC4105A IC₅₀ MerTK 4.6 nM Tyro3 27 nM Flt3 11 nM UNC4106A IC₅₀ MerTK 3.2 nM Tyro3 22 nM Flt3 8.9 nM Axl 47 nM UNC4109A IC₅₀ MerTK 2.9 nM Tyro3 28 nM Flt3 9.2 nM Axl 119 nM UNC4110A IC₅₀ MerTK 2.3 nM Tyro3 19 nM Flt3 4.5 nM UNC4111A IC₅₀ MerTK 2.5 nM Tyro3 20 nM Flt3 6.4 nM UNC4112A IC₅₀ MerTK 3.3 nM Tyro3 19 nM Flt3 5.3 nM Axl 32 nM UNC4113A IC₅₀ MerTK 2.4 nM Tyro3 18 nM Flt3 5.6 nM Axl 55 nM UNC4160A IC₅₀ MerTK 0.67 nM Tyro3 10 nM Axl 19 nM Flt3 4.6 nM UNC4166A IC₅₀ MerTK 1 nM Tyro3 9.4 nM Axl 13 nM Flt3 4.8 nM UNC4167A IC₅₀ MerTK 0.86 nM Tyro3 6.4 nM Axl 18 nM Flt3 2 nM UNC4168A IC₅₀ MerTK 1.2 nM Tyro3 12 nM Axl 23 nM Flt3 12 nM UNC4196A IC₅₀ MerTK 4.8 nM Tyro3 58 nM Axl 263 nM Flt3 15 nM UNC4169A IC₅₀ MerTK 0.81 nM Tyro3 3.9 nM Axl 9.6 nM Flt3 2.4 nM UNC4220A IC₅₀ MerTK 17 nM Tyro3 68 nM Axl 122 nM Flt3 28 nM UNC4221A IC₅₀ MerTK 6.8 nM Tyro3 43 nM Axl 104 nM Flt3 14 nM UNC4279A IC_(SO) MerTK 4.6 nM Tyro3 42 nM Axl 67 nM Flt3 12 nM UNC4281A IC₅₀ MerTK 11 nM Tyro3 65 nM Axl 98 nM Flt3 15 nM UNC4222A IC₅₀ MerTK 2.9 nM Tyro3 16 nM Axl 39 nM Flt3 2.6 nM UNC4230A IC₅₀ MerTK 81 nM Tyro3 734 nM Axl 1764 nM Flt3 271 nM UNC4335A Axl 137 nM IC₅₀ MerTK 5.3 nM Tyro3 56 nM Flt3 12 nM UNC4336A Tyro3 13 nM Axl 40 nM IC₅₀ MerTK 1.9 nM Flt3 1.8 nM UNC4337A Tyro3 66 nM Axl 74 nM IC₅₀ Mer 4.4 nM Flt3 7.8 nM UNC4338A Axl 42 nM IC₅₀ MerTK 2.9 nM Tyro3 20 nM Flt3 5.4 nM UNC4339A Axl 39 nM IC₅₀ MerTK 3.3 nM Tyro3 22 nM Flt3 8.7 nM UNC4340A Tyro3 8.5 nM Axl 9.2 nM IC₅₀ Mer 1.1 nM Flt3 2.0 nM UNC4354A Flt3 2.6 nM IC₅₀ MerTK 1.4 nM Tyro3 24 nM Axl 27 nM UNC4356A Flt3 3.3 nM IC₅₀ MerTK 1.3 nM Tyro3 56 nM Axl 38 nM UNC4358A Flt3 7.2 nM IC₅₀ MerTK 2.2 nM Tyro3 42 nM Axl 24 nM UNC4387A IC₅₀ MerTK 72 nM Tyro3 488 nM Axl 320 nM Flt3 9.3 nM UNC4386A IC₅₀ MerTK 2.5 nM Tyro3 53 nM Axl 53 nM Flt3 3.6 nM

Example 25 Efficacy of a Novel Small Molecule MerTK Receptor Tyrosine Kinase Inhibitor in B-RAF Wild-Type and B-RAF Mutant Melanoma Cell

A MERTK-selective small-molecule tyrosine kinase inhibitor (TKI) is evaluated in preclinical models of melanoma, both alone and in combination with vemurafenib (a mutant B-RAF TKI). B-RAF wild-type (HMCB) and B-RAF mutant (G361) cell lines are treated with Mer TKI or vehicle. Downstream signaling is evaluated by immunoblotting, and induction of apoptosis is determined by flow cytometry in cells stained with YO-PRO®-1 iodide and propidium iodide. Alternatively, cells are seeded in media containing Mer TKI or vehicle and colony formation is determined.

Example 26 Inhibition of Murine Melanoma Growth by a Small Molecule Mer Tyrosine Kinase Inhibitor (Mer TKI)

In this example, the activity of a MerTK inhibitor is examined on tumor growth in autochthonous murine tumor models. Mer TKI is assessed in immune-competent, genetically engineered murine models (GEMMs). Activity is tested in RAS-driven, INK4a/Arf null melanoma GEMM (TRIA) mice. The efficacy of 15 chemotherapeutic and/or targeted regimens in a large (>220) cohort of TRIA mice has previously been tested (Clinical Cancer Research 18:5290, 2012). The overall response is 10% (partial responses and stable disease). There are no complete responses. A combination of MEK (AZD 6244) and PI3K/mTOR (BEZ235) inhibitors are the most active previous regimen (responses seen in 9/18 mice=50%, with 0 CRs) with moderate toxicity.

Example 27 Cell Killing by Mer TKIs in Combination with FGFR Inhibition

In this study, the interaction between a novel MerTK-selective small molecule tyrosine kinase inhibitor (TKI) and AZD-4547, an FGFR TKI, in NSCLC cell lines is studied. Colo699 (MerTK+, FGFR+) and H226 (MerTK+, FGFR+) NSCLC cells are cultured for 14 days in soft agar in the presence of Mer TKI and/or AZD-4547, alone or in combination, and colonies are stained and counted. Changes in the activity of downstream signaling pathways, including PI3K/AKT, MEK/ERK, and STAT proteins are evaluated by immunoblotting.

Example 28 Inhibition of Mer Tyrosine Kinase with a Novel Small Molecule Inhibitor in Mouse Models of all

In this example, preclinical testing of Mer TKIs as a potential therapy for MERTK-expressing ALL is disclosed. Mer TKI inhibition of phosphorylation/activation of MerTK is tested in 697 B-ALL cells. Mer TKIs are tested in several mouse models, including an orthotopic B-ALL xenograft model of minimal residual disease and a similar model of existent disease in which leukemia is established for 14 days prior to initiation of treatment. In both models, tumor burden is measured by bioluminescent imaging.

Example 29 Inhibition of Mer Tyrosine Kinase with a Novel Small Molecule Inhibitor in Pre-Clinical Models of Non-Small Cell Lung Cancer

The effects of Mer TKI treatment on activation of MerTK and related members of the TAM-family of kinases, Axl and Tyro3, and effects on downstream proliferative and pro-survival signaling pathways are analyzed by immunoblot. In addition, Mer TKI-mediated anti-tumor activity is determined in a panel of NSCLC cell lines using soft-agar and clonogenic assays. Cells are stained with YoPro-1-iodide and propidium iodide dyes and induction of apoptosis is determined using flow cytometry. Finally, a subcutaneous murine xenograft model is employed to determine therapeutic effects in vivo.

Example 30 A Dual FLT-3 and Mer Tyrosine Kinase Small Molecule Inhibitor in Acute Myeloid Leukemia Cell Lines and Patient Samples

FLT-3 and Mer tyrosine kinases have been previously identified as potential targets in the treatment of acute myeloid leukemia (AML). Expression of FLT-3 internal tandem duplication (ITD) occurs in ˜30-40% of AML patient samples and MerTK overexpression has been detected in ˜80-100%. In this example, a novel small molecule inhibitor is tested for activity against both of these kinases and the growth inhibition or apoptosis of cell lines and patient myeloblasts is examined. In these studies, the effects of treatment with MER-TKI are analyzed in FLT3-ITD-positive (Molm-13 and MV4;11) and MERTK-positive (Kasumi-1 and U937) AML cell lines and in primary AML patient samples with variable expression of FLT3-ITD and MerTK. AML cell lines are also stained with Yo-Pro-1 iodide and propidium iodide and analyzed by flow cytometry to determine induction of apoptosis in response to treatment with Mer TKI. Primary patient samples that are MerTK and/or FLT3-ITD positive are analyzed in similar assays.

Example 31 Targeted Inhibition of Mer Tyrosine Kinase in the Tumor Microenvironment in a Mouse Model of Breast Cancer

To further investigate the utility of MerTK inhibition in the tumor microenvironment as a therapeutic strategy, the efficacy of a Mer TKI is evaluated in immunocompetent C57Bl/6 mice implanted orthotopically with PyVmT mammary gland tumor cells. These PyVmT tumors cells do not express MerTK, AXL or TYRO3.

Example 32 Murine FeCl₃-Induced Carotid Artery Thrombosis Model

6-12-week old C57BL/6 mice (The Jackson Laboratory, Bar Harbor, Me.), are fed low-soy laboratory chow to prevent interactions from genestein, a phytoestrogen with tyrosine kinase inhibitor activity. Approximately equal numbers of male and female mice are used for all experiments to limit any potential skewing of results by sex-based differences in thrombosis. The mice are anesthetized with intraperitoneal sodium pentobarbital (60-90 mg·kg⁻¹ loading dose, 10 to 20 mg/kg⁻¹ maintenance dose as needed to maintain adequate anesthesia as measured by paw pressure response). The mice are then fixed in the supine position to a polycarbonate experimental platform under a dissecting microscope (Olympus SZ61 Infinity Lite, Olympus Equipment). A rectal temperature probe is used in conjunction with a heating pad to monitor and maintain temperature at 37±1° C. A 2 cm vertical midline ventral cervical incision is made to expose the trachea, which is then horizontally incised and cannulated with a rigid endotracheal tube (Harvard MiniVent type 845, Harvard Apparatus) secured with a 4-0 silk tie, and attached to a ventilator (Harvard MiniVent type 845, Harvard Apparatus), which delivered a 200 μL stroke volume and 80 breaths per minute. The carotid artery is exposed by dissection, allowing for attachment of a microvascular ultrasonic flow probe (Transonic Flowprobe, Transonic Systems, Ithaca, N.Y.), and the cavity is flooded with NaCl to prevent tissue dehydration. A 1 mm×5 mm strip of Parafilm (Pechiney Plastic Packaging, Chicago, Ill.) is placed perpendicular to, and immediately posterior to, the artery to separate it from other cavity tissue. NaCl (negative control), Mer TKI (3 mg/kg in NaCl), 2 μM abciximab (positive control), HD ADPis in NaCl (3 mg/kg MRS2179+3 mg/kg 2-MeSAMP), LD ADPis (1.5 mg/kg MRS2179+1.5 mg/kg 2-MeSAMP), or a combination of Mer TKI and LD ADPis are injected and allowed to circulate for 30 minutes. The cavity is then dried and a 1.2 mm diameter circle of filter paper (Whatman Ltd, Chippenham, Wiltshire, UK) is saturated with 6% FeCl₃ (˜60 μM, Fisher) for 10 seconds, and placed on the artery, proximal to the ultrasound probe, for 3 minutes to create the injury. Then, the Parafilm and filter paper are removed, the cavity is flooded with saline, and the flow probe readout is analyzed using LabChart software (AD Instruments, CO Springs, Colo.). Elapsed Time To First (initial) artery Occlusion (TTFO, mean blood flow of 0 mL/min flow for >30 seconds), and total Duration Of Occlusion time (D00, mean blood flow<20% of pre-FeCl₃ baseline) is measured during the 60 minutes following FeCl₃ application. Values are expressed as mean+/−SEM, with significance determined by unpaired, two-tailed Student's t-test.

Example 33 Effects of FLT3 and MerTK Inhibitors on MerTK Phosphorylation and Downstream Signaling in Acute Myeloid Leukemia Cell Lines

Two cell lines known to express a FLT3-ITD mutation (Molm14 and MV4;11) are treated with a novel FLT3 inhibitor which has high specificity for FLT3. The MV4;11 cell line has low MerTK expression, while the Molm14 cell line does not express MerTK. Immunoprecipitation of FLT3-ITD positive AML cell lines after 1 h treatment with a MerTK inhibitor is analyzed for phosphorylation of FLT3 (pFLT3) in comparison to total FLT3. Phosphorylation of downstream signaling proteins STATS, AKT, and ERK1/2 in comparison to DMSO and control TKI are also analyzed. In addition, an AML cell line that expresses MerTK and does not have activating mutations in FLT3 (U937, Kasumi-1) is also used to determine abrogation of activation of intracellular signaling pathways downstream of FLT3 and MerTK, including AKT and ERK1/2, when treated with MerTK inhibitors. Signaling in AML cell lines is analyzed after 1 hr treatment with MerTK inhibitors. Whole cell lysates or IPs are resolved on 8% Tris-Glycine SDS-PAGE gels, then transferred to a nitrocellulose membrane, which are probed for phospho-proteins. Blots are then stripped and re-probed for the total protein, or actin (loading control).

Example 34 Effect of MerTK Inhibitors on Apoptosis in Acute Myeloid Leukemia Cell Lines

AML cell lines are plated in equal number in soft agar, then colony number analyzed after incubation at 37° C. for 14 days. Colonies are counted using a Gel Count automated colony counter. AML cell lines are treated for 72 h with MerTK and apoptosis is analyzed after staining with Yo-Pro-1 iodide and propidium iodide and undergoing flow cytometric analysis.

Example 35 MerTK Inhibitors in a Molm14 Xenograft Model (FLT3-ITD AML)

A Molm14 xenograft is established by injection of 2.5×10⁶ cells into NSG mice via tail vein. On day 4 after injection mice are started on daily therapy with a MerTK inhibitor or saline via oral gavage. Mice are treated through day 100 then observed for relapse.

Example 36 MerTK Inhibitors in a Patient-Derived Xenograft Model (FLT3-ITD AML)

A patient-derived xenograft model is established with cells from a patient with FLT3-ITD+AML. NSG mice are sublethally irradiated and then 5×10⁶ cells are injected via tail vein. Mice are started on therapy in the same fashion as described in Example 13 once peripheral blast counts reached ˜10%.

Example 37 MerTK Inhibitors in FLT3-ITD AML Cell Lines with AC220-Resistance Mutations (D835Y and F691L)

Two cell line derivatives of the human FLT3-ITD AML cell line Molm14, which acquired either the D835Y (activation loop) or F691L (gatekeeper) mutation after selection in escalating doses of the FLT3 inhibitor AC220, are used to test the activity of MerTK inhibitors against clinically relevant FLT3 point mutations. Cells are analyzed for viability after 48 hours of culture in Molm14, Molm14:D835Y, and Molm14:F691L after treatment with a MerTK inhibitor. Phosphorylation is analyzed in Molm14, Molm14:D835Y, and Molm14:F691L after treatment with a MerTK inhibitor. Cell lines are also analyzed for resistance to treatment with AC220 at concentrations (e.g. 20-fold higher) than the inhibitory concentration in the parental line.

Example 38 MerTK Inhibitors in Molm14 Xenograft Model (FLT3-ITD AML) with AC220-Resistance Mutations (D835Y and F691L)

A Molm14:D835Y xenograft model is established by injection of 2.5×10⁶ Molm14:D835Y cells into NSG mice via tail vein. The D835Y mutation in the activation loop confers resistance to the FLT3 inhibitor AC220. On day 4 after injection, mice are started on daily therapy with a MerTK inhibitor, 10 mg/kg AC220, or saline via oral gavage. Mice are treated through day 100 then observed for relapse.

The foregoing is illustrative of the present invention, and is not to be construed as limiting thereof. The invention is defined by the following claims, with equivalents of the claims to be included therein. 

The invention claimed is:
 1. A method for treating a host with an infectious disease, comprising administering an effective amount of a compound of Formula I or II:

wherein: ring A is a 5- or 6-membered heteroaryl group; dashed lines are optional double bonds; X is N or O; Y is a carbon atom or an S or N heteroatom in ring A in any suitable location; R¹ is —R⁵R⁶, where R⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group and R⁶ is cycloalkyl, piperidyl, heterocycloalkyl, aryl, heteroaryl, alkylcycloalkyl, alkylheterocycloalkyl, alkylaryl, alkylheteroaryl or alkyl, and wherein R⁶ is optionally substituted one, two or three times with independently selected polar groups; R² is —R⁷R⁸, where R⁷ is a covalent bond or C₁ to C₃ alkyl and R⁸ is cycloalkyl, heterocycloalkyl, aryl, heteroaryl or alkyl, and wherein R⁸ is optionally substituted one, two or three times with independently selected polar groups; R³ is selected from the group consisting of H, alkyl, aryl, arylalkyl; cycloalkylalkyl, heterocycloalkylalkyl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times with independently selected polar groups; or R² and R³ together form a linking group; R⁴ is H, loweralkyl, halo, or loweralkoxy; or a pharmaceutically acceptable salt thereof.
 2. A method for treating a host with an infectious disease, comprising administering an effective amount of a compound of the formula:

wherein: R¹¹ is —R¹⁵R¹⁶, where R¹⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R¹⁶ is hydrogen, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocycloalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, heteroarylalkyl, hydroxyl, alkoxy, haloalkoxy, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, or acyloxy, and wherein R¹⁶ is optionally substituted one, two, three, four or five times; m=0, 1, 2 or 3; R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, alkoxyalkyl, hydroxyalkyl or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times; R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocyclic ring that can be optionally substituted; R¹³ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; or R¹² and R¹³ together form a linking group; R⁴ is H, loweralkyl, halo, or loweralkoxy; R⁹ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; R¹¹ and R¹⁴ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted; R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted; R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl; R¹⁴ is hydrogen, alkyl or alkylaryl; with the proviso: wherein if R⁹ and R¹³ with the nitrogen to which they are bonded do not form a heterocyclic group then one of R⁹ or R¹³ is hydrogen; and wherein if R¹⁰ and R¹² with the nitrogen to which they are bonded do not form a heterocyclic group then one of R¹⁰ or R¹² is hydrogen; and wherein if R¹² and R¹³ together form a linking group, then both R⁹ and R¹³ are hydrogen;
 3. A method for treating a host with an infectious disease, comprising administering an effective amount of a compound of the formula:

wherein: ring A is a 5- or 6-membered heteroaryl group (for example, pyridyl, pyrimidyl, thiazol, furanyl, pyridazinyl, pyrazinyl, imidazol, etc.). The dashed lines are optional double bonds. X is N or O. Y is a carbon atom or an S or N heteroatom in ring A in any suitable location. R¹⁹ is —R²⁰R²¹, where R²⁰ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R²¹ is hydrogen, alkyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocyclolalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, alkylheteroaryl, halo, hydroxyl, alkoxy, haloalkoxy, mercapto, alkyl-S(O)_(m)—, haloalkyl-S(O)_(m)—, alkenyl-S(O)_(m)—, alkynyl-S(O)_(m)—, cycloalkyl-S(O)_(m)—, cycloalkylalkyl-S(O)_(m)—, aryl-S(O)_(m)—, arylalkyl-S(O)_(m)—, heterocyclo-S(O)_(m)—, heterocycloalkyl-S(O)_(m)—, amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstitutedamino, acylamino, acyloxy, ester, amide, COOH, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, and wherein R²¹ is optionally substituted one, two or three times; or two adjacent R¹⁹ groups can form an aryl or heteroaryl ring with the carbons that they are bonded to and can be optionally substituted; R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl hydroxyalkyl, alkoxyalkyl, or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times; R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocyclic ring that can be optionally substituted; R¹³ is selected from the group consisting of H, alkyl, hydroxyalkyl, aryl, arylalkyl; cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; or R¹² and R¹³ together form a linking group; R⁴ is H, loweralkyl, halo, or loweralkoxy; R⁹ is selected from the group consisting of H, alkyl, aryl, arylalkyl; cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; or R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted; R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl; m=0, 1, 2 or 3; p=0, 1 or 2; or its pharmaceutically acceptable salt.
 4. The method of claim 1, wherein the infectious disease is a viral infection.
 5. The method of claim 2, wherein the infectious disease is a viral infection.
 6. The method of claim 3, wherein the infectious disease is a viral infection.
 7. The method of claim 1, wherein the infectious disease is a bacterial infection.
 8. The method of claim 2, wherein the infectious disease is a bacterial infection.
 9. The method of claim 3, wherein the infectious disease is a bacterial infection.
 10. The method of claim 4, 5 or 6, wherein the virus is selected from the group consisting of wherein the virus is selected from the group consisting of a Flavivirus, Hepacivirus, Pegivirus, Pestivirus, Filovirus, Togavirus, Coronavirus, Orthomyxovirus, Paramyxovirus, Calicivirus, and Lentivirus.
 11. The method of claim 10, wherein the virus is Chikungunya.
 12. The method of claim 10, wherein the virus is HCV.
 13. The method of claim 10, wherein the virus is HIV.
 14. The method of claim 7, 8 or 9, wherein the bacterial disease is selected from the group consisting of Escherichia coli, Staphylococcus aureus, Enterococcus faecalis, and Streptococcus pneumoniae.
 15. A method for treating a host with a medical disorder in need of immunosuppressive adjunctive therapy in combination with a direct acting drug for the medical disorder, comprising administering an adjunctively immunosuppressive effective amount of a compound of the formula:

wherein: ring A is a 5- or 6-membered heteroaryl group; dashed lines are optional double bonds; X is N or O; Y is a carbon atom or an S or N heteroatom in ring A in any suitable location; R¹ is —R⁵R⁶, where R⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group and R⁶ is cycloalkyl, piperidyl, heterocycloalkyl, aryl, heteroaryl, alkylcycloalkyl, alkylheterocycloalkyl, alkylaryl, alkylheteroaryl or alkyl, and wherein R⁶ is optionally substituted one, two or three times with independently selected polar groups; R² is —R⁷R⁸, where R⁷ is a covalent bond or C₁ to C₃ alkyl and R⁸ is cycloalkyl, heterocycloalkyl, aryl, heteroaryl or alkyl, and wherein R⁸ is optionally substituted one, two or three times with independently selected polar groups; R³ is selected from the group consisting of H, alkyl, aryl, arylalkyl; cycloalkylalkyl, heterocycloalkylalkyl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times with independently selected polar groups; or R² and R³ together form a linking group; R⁴ is H, loweralkyl, halo, or loweralkoxy; or a pharmaceutically acceptable salt thereof.
 16. A method for treating a host with a medical disorder in need of immunosuppressive adjunctive therapy in combination with a direct acting drug for the medical disorder, comprising administering an adjunctively immunosuppressive effective amount of a compound of the formula:

wherein: R¹¹ is —R¹⁵R¹⁶, where R¹⁵ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R¹⁶ is hydrogen, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocycloalkyloxy, aryl, arylalkyl, aryloxy, arylalkyloxy, heteroaryl, heteroarylalkyl, hydroxyl, alkoxy, haloalkoxy, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, or acyloxy, and wherein R¹⁶ is optionally substituted one, two, three, four or five times; m=0, 1, 2 or 3; R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, alkoxyalkyl, hydroxyalkyl or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times; R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocyclic ring that can be optionally substituted; R¹³ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, hydroxyalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; or R¹² and R¹³ together form a linking group; R⁴ is H, loweralkyl, halo, or loweralkoxy; R⁹ is selected from the group consisting of H, alkyl, alkenyl, alkynyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; R¹¹ and R¹⁴ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted; R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted; R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl; R¹⁴ is hydrogen, alkyl or alkylaryl; with the proviso: wherein if R⁹ and R¹³ with the nitrogen to which they are bonded do not form a heterocyclic group then one of R⁹ or R¹³ is hydrogen; and wherein if R¹⁰ and R¹² with the nitrogen to which they are bonded do not form a heterocyclic group then one of R¹⁰ or R¹² is hydrogen; and wherein if R¹² and R¹³ together form a linking group, then both R⁹ and R¹³ are hydrogen;
 17. A method for treating a host with a medical disorder in need of immunosuppressive adjunctive therapy in combination with a direct acting drug for the medical disorder, comprising administering an adjunctively immunosuppressive effective amount of a compound of the formula:

wherein: ring A is a 5- or 6-membered heteroaryl group (for example, pyridyl, pyrimidyl, thiazol, furanyl, pyridazinyl, pyrazinyl, imidazol, etc.). The dashed lines are optional double bonds. X is N or O. Y is a carbon atom or an S or N heteroatom in ring A in any suitable location. R¹⁹ is —R²⁰R²¹, where R²⁰ is a covalent bond, C₁ to C₃ alkyl or a linker group (for example, sulfonamide, ether, ester, amine, amide, etc.) and R²¹ is hydrogen, alkyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, alkenyl, alkenyloxy, alkynyl, alkynyloxy, cycloalkyl, cycloalkylalkyl, cycloalkoxy, cycloalkylalkyloxy, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heterocyclooxy, heterocyclolalkyloxy, aryl, arylalkyl, acyloxy, arylalkyloxy, heteroaryl, alkylheteroaryl, halo, hydroxyl, alkoxy, haloalkoxy, mercapto, alkyl-S(O)_(m)—, haloalkyl-S(O)_(m)—, alkenyl-S(O)_(m)—, alkynyl-S(O)_(m)—, cycloalkyl-S(O)_(m)—, cycloalkylalkyl-S(O)_(m)—, aryl-S(O)_(m)—, arylalkyl-S(O)_(m)—, heterocyclo-S(O)_(m)—, heterocycloalkyl-S(O)_(m)—, amino, carboxy, alkylamino, —(CH₂)_(m)—NH(CH₂)_(m)CH₃, —(CH₂)_(m)—NH(CH₂)_(m)OH, alkenylamino, alkynylamino, haloalkylamino, cycloalkylamino, cycloalkylalkylamino, arylamino, arylalkylamino, heterocycloamino, heterocycloalkylamino, disubstitutedamino, acylamino, acyloxy, ester, amide, COOH, sulfonamide, urea, alkoxyacylamino, aminoacyloxy, and wherein R²¹ is optionally substituted one, two or three times; or two adjacent R¹⁹ groups can form an aryl or heteroaryl ring with the carbons that they are bonded to and can be optionally substituted; R¹² is —R¹⁷R¹⁸, where R¹⁷ is a covalent bond or C₁ to C₃ alkyl and R¹⁸ is cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl hydroxyalkyl, alkoxyalkyl, or alkyl, and wherein R¹⁸ is optionally substituted one, two or three times; R¹⁰ and R¹² together with the nitrogen to which they are bonded can form a heterocyclic ring that can be optionally substituted; R¹³ is selected from the group consisting of H, alkyl, hydroxyalkyl, aryl, arylalkyl; cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; or R¹² and R¹³ together form a linking group; R⁴ is H, loweralkyl, halo, or loweralkoxy; R⁹ is selected from the group consisting of H, alkyl, aryl, arylalkyl; cycloalkyl, cycloalkylalkyl, heterocyclo, heterocycloalkyl, alkylheterocycloalkyl, heteroaryl, heteroarylalkyl, and alkoxyalkyl, each of which is optionally substituted one, two or three times; or R⁹ and R¹³ together with the nitrogen to which they are bonded can form a heterocyclic group that can be optionally substituted; R¹⁰ is hydrogen, alkyl, alkoxyalkyl or alkylaryl; m=0, 1, 2 or 3; p=0, 1 or 2;
 18. A method for treating a host with acute myeloid leukemia (AML) or acute lymphoblastic leukemia (ALL) comprising administering an effective amount of the compound of claim
 1. 19. A method for treating a host with acute myeloid leukemia or acute lymphoblastic leukemia comprising administering an effective amount of the compound of claim
 2. 20. A method for treating a host with acute myeloid leukemia or acute lymphoblastic leukemia comprising administering an effective amount of the compound of claim
 3. 21. The method of claim 18, wherein the AML or ALL is resistant to prior drug therapy.
 22. The method of claim 19, wherein the AML or ALL is resistant to prior drug therapy.
 23. The method of claim 18 or 19 wherein the AML contains a mutation within the FLT3-TKD at amino acid F691 or D835. 